Medical devices, 2018
Shortlist up to four to read them side by side.
3,757 medical device recalls FDA’s Enforcement Report published in 2018, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 6, 2026.
3,757of 3,757 medical device recallsshown with your filters
The list
- Medical device recall CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a Two analgesic gas delivery system oxygen/nitrous oxide mixers were reported to have delivered higher levels of nitrous oxide than specification during routine… Class IIFDA’s classAug 29, 2018in FDA’s Enforcement Report47 statesnamed in where it went PublishedAug 29, 2018ClassClass IIStatusTerminatedWhereAlaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia
- Medical device recall CIVCO lnfiniti Needle Guide Bracket A cover failed leak testing during validation testing of new needle guides from a replacement tool. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedAug 29, 2018ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Georgia, Iowa, Illinois, Kentucky, Massachusetts, New Jersey, New York, Rhode Island and Texas named
- Medical device recall Vertebral Motion Analyzer (VMA), 2.3.250 This email is to provide notification that, due to a software bug that has been corrected, the Radiological Read Report for the VMA test(s) contained an error. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Vertebral Motion Analyzer (VMA), VMA DataLink Software.2.3.231, 2.3.232 Ortho Kinematics, Inc. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254 Ortho Kinematics notified customers that errors were contained in Radiological Read Report and VMA Report for the VMA test. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of multiple adult,… Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Philips SureSigns VS3 Vital Signs Monitor, 863069 863070 863071 863072 863073 863074 The SureSigns VS3… Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Philips SureSigns VS4 Vital Signs Monitor, 863283 863286 The SureSigns VS4 vital signs monitor is for use by… Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Philips SureSigns VM 3/4/6/8 Patient Monitors, 863063 863064 863065 863066 863068 863077 863085 863086 863317… Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2 vital signs… Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous… Punch may have a burr in one section of the joint and when the punch is open, there is an increase potential for injury. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNot namedno state, in where it went PublishedAug 29, 2018ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power Johnson and Johnson Vision Care received a number of reports of a partially formed contact lens, which appears to the customer or consumer as visibly smaller… Class IIFDA’s classAug 29, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 22 states named PublishedAug 29, 2018ClassClass IIStatusTerminatedWhereNationwide, and California, Connecticut, Florida, Georgia, Iowa, Illinois, Massachusetts, Maryland, Maine, Missouri, North Carolina, Nebraska, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, Tennessee, Texas, Utah and Virginia named
- Medical device recall MOSAIQ Oncology Information System Order Status Remains Approved When Should Indicate Complete. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement Report40 statesnamed in where it went PublishedAug 29, 2018ClassClass IIStatusTerminatedWhereAlaska, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Idaho, Illinois, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Immunoscan CCPlus test kit is an enzyme-linked immunosorbent assay (ELISA) for qualitative and… Decreasing performance overtime. Class IIFDA’s classAug 29, 2018in FDA’s Enforcement Report2 statesnamed in where it went PublishedAug 29, 2018ClassClass IIStatusTerminatedWhereMinnesota and Texas
- Medical device recall is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of autoantibodies… Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class IIIFDA’s classAug 29, 2018in FDA’s Enforcement ReportMinnesotathe one state its words name PublishedAug 29, 2018ClassClass IIIStatusTerminatedWhereMinnesota
- Medical device recall is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM… Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class IIIFDA’s classAug 29, 2018in FDA’s Enforcement ReportMinnesotathe one state its words name PublishedAug 29, 2018ClassClass IIIStatusTerminatedWhereMinnesota
- Medical device recall is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM… Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class IIIFDA’s classAug 29, 2018in FDA’s Enforcement ReportMinnesotathe one state its words name PublishedAug 29, 2018ClassClass IIIStatusTerminatedWhereMinnesota
- Medical device recall is a qualitative indirect enzyme immunoassay enzyme-linked immunosorbent assay (ELISA) for the detection, in… Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin. Class IIIFDA’s classAug 29, 2018in FDA’s Enforcement ReportMinnesotathe one state its words name PublishedAug 29, 2018ClassClass IIIStatusTerminatedWhereMinnesota
- Medical device recall Arkon Anesthesia Delivery System with Arkon Software Version 2.70, Display Unit Assembly 650-1769-00… Arkon Anesthesia Delivery System may go into a failed state (mechanical ventilation ceases) while the machine is in use or while idle. FDA Class I, its most serious class Class IFDA’s class (needs attention)Aug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 14 states named PublishedAug 22, 2018ClassClass IStatusTerminatedWhereNationwide, and Colorado, Illinois, Indiana, Louisiana, Massachusetts, Maine, Montana, Nebraska, New Mexico, New York, Pennsylvania, Puerto Rico, Texas and Wyoming named
- Medical device recall 1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body. Supplier manufacturing defect with the syringe plunger tip. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, North Dakota, New Jersey, New Mexico, New York, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia named
- Medical device recall Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone… Component of the Lap-Band system was missing from the package Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report11 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereFlorida, Illinois, Louisiana, Michigan, Missouri, North Carolina, New York, Tennessee, Texas, Virginia and West Virginia
- Medical device recall AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device, Patient mount: a) Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without Transducer confirmed the potential for a pinhole breach in the sterile barrier. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall G8 Automated HPLC Analyzer: HLC-723G8-ST, 021560 HbAE is known to interfere with the HbA1c assay on the current version of software, Ver. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage: Indicated for the delivery of… QFix has advised Mevion Medical Systems that they are identifying unauthorized combinations of QFix Couch Tops with non-QFix devices in clinical use. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia, Florida, Missouri, New Jersey, Ohio and Oklahoma named
- Medical device recall Artis Q. angiography system. Model 10848280, 10848281, 10848282, 10848283, 10848353, 10848354 & 10848355… Potential hardware issue which may cause thermal effects and possible damage to system parts. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product Usage: Artis is a family of… Potential hardware issue which may cause thermal effects and possible damage to system parts. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall EZ Single Cytofunnel Brown, A78710004 Product Usage: The EZ Single Cytofunnel with Brown filter papter are… Mislabeled product Class IIIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIIStatusTerminatedWhereNationwide
- Medical device recall CDI Blood parameter monitoring system 500 H/SAT H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat population, which has resulted in an increase of Hybrids failing the H/Sat Color Chip Test… Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arizona, California, Florida, Georgia, Illinois, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Mexico, New York, Ohio, South Carolina, Tennessee, Texas, Washington and West Virginia named
- Medical device recall Monitor with one Blood Parameter Module and one HSat Probe H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat population, which has resulted in an increase of Hybrids failing the H/Sat Color Chip Test… Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arizona, California, Florida, Georgia, Illinois, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Mexico, New York, Ohio, South Carolina, Tennessee, Texas, Washington and West Virginia named
- Medical device recall Clarity Urocheck 10SG Urinalysis Strips Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are not compatible for use in the Clarity Urocheck 120 Urine Analyzers, due to lack of… Class IIIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedAug 22, 2018ClassClass IIIStatusTerminatedWhereNationwide, and Arizona, Massachusetts, South Carolina and Washington named
- Medical device recall TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO,COC20,METSO, OPl40,OXY20,THC2S) Product Usage: T-Cube¿… GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral Fluid Test Cube the potential for failure of the saliva collection device. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportVirginiathe one state its words name PublishedAug 22, 2018ClassClass IIStatusOngoingWhereVirginia
- Medical device recall TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO, BARGO, BZ030,COC20,MDMA100,METSO, MTD30,OPl40,OXY20,… GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral Fluid Test Cube the potential for failure of the saliva collection device. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportVirginiathe one state its words name PublishedAug 22, 2018ClassClass IIStatusOngoingWhereVirginia
- Medical device recall TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO, BARGO, SUPS, BZ030, COC20,MDMAlOO, METSO,… GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral Fluid Test Cube the potential for failure of the saliva collection device. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportVirginiathe one state its words name PublishedAug 22, 2018ClassClass IIStatusOngoingWhereVirginia
- Medical device recall Improve Blood Collection Sets with Multiple Sample Luer Adapter - Sterile/EO Product Usage: The Blood… Complaints about the needle is not smooth, with discoloration, a kind of gel agglomeration on the needle tip. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedAug 22, 2018ClassClass IIStatusOngoingWherePuerto Rico
- Medical device recall VentriClear Ventricular Drainage Catheter Set This lot of VentriClear failed endotoxin testing. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportIndianathe one state its words name PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereIndiana
- Medical device recall MegaPower Electrosurgical Generator If two devices are plugged into the same channel/port in the generator, both devices activate. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NxStage Express Fluid Warmer (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A) Product Usage: The NxStage… There is a potential risk of electrical fire when fluid leaks into the power receptacle on the back of the warmer. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Rio System Irrigation Clip Out of tolerance. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement ReportNationwideFDA’s word, and 41 states named PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and Wyoming named
- Medical device recall Hamilton-C1 Ventilator Unit Product Usage: The HAMILTON-C1 ventilator is intended to provide positive… An out of specification component on the control board may cause the ventilator to open the inspiratory channel and the expiratory valve. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report9 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereCalifornia, Colorado, Illinois, Louisiana, Minnesota, New York, Oklahoma, Virginia and Wisconsin
- Medical device recall Hamilton-C3 Ventilator Unit Product Usage: The HAMILTON-C3 ventilator is intended to provide positive… An out of specification component on the control board may cause the ventilator to open the inspiratory channel and the expiratory valve. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report9 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereCalifornia, Colorado, Illinois, Louisiana, Minnesota, New York, Oklahoma, Virginia and Wisconsin
- Medical device recall 20 cm (8”) PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer single… ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall 165 cm (65”) PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a… ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall 30 cm (12”) PUR Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, 2 NanoClave, Rotating Luer a single… ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall DISTALE - 203 cm ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall 216 cm (85”) PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, MicroClave… ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall 43 cm (17”) Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, 0.2 Micron Filter, 2… ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall 18 cm (7”) PUR Smallbore Ext Set w/6-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer. ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
- Medical device recall 28 cm (11”) PUR Bifuse Ext Set w/6-Port NanoClave Manifold, Check Valve, 2 NanoClave, Rotating Luer. ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Class IIFDA’s classAug 22, 2018in FDA’s Enforcement Report7 statesnamed in where it went PublishedAug 22, 2018ClassClass IIStatusTerminatedWhereArizona, Massachusetts, North Carolina, Ohio, Texas, Virginia and Washington
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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