Medical devices, 2024
Shortlist up to four to read them side by side.
3,394 medical device recalls FDA’s Enforcement Report published in 2024, 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.
3,394of 3,394 medical device recallsshown with your filters
The list
- Medical device recall Medline procedural kits labeled as: CIRCUMCISION TRAY, Pack Number DYNDA2271 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) BOTOX KIT - CHRONIC MIGRAINE, Pack Number DYKM2000 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) DRAWER 3 LAB DRAW & IV START, Pack Number ACC010417 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) ARTHROGRAM TRAY, Pack Number MNS11965A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: UMBILICAL LINE KIT W/FOAM, Pack Number DYNDL1588A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: ARTHROGRAPH TRAY, Pack Number MNS12670A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) CIRCUMCISION TRAY, Pack Number CIT6715 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) CIRCUMCISION TRAY, Pack Number CIT6715 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) BABY ADMIT, Pack Number DYKB1011C Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) GLMI ARTHROGRAM KIT:PCL, Pack Number SPEC0300B Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: NEURO TRAY, Pack Number DYNJ55909B Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) INFANT DELIVERY KIT , Pack Number DYKM1426 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline Procedure kits labeled as: 1) CIRCUMCISION SET, Pack Number CIT6335 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) SR C SECTION, Pack Number DYNJ908584 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) LEEP PACK, Pack Number DYNJ40348G Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) ALL DOC EYE PACK, Pack Number DYNJ51654A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Medline procedural kits labeled as: 1) AFCH ANTERIOR SEGMENT PK, Pack Number DYNJ63330B Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits labeled as: 1) BIOPSY KIT, Pack Number DYNDA1466A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits, labeled as: 1) 6” FEMORAL ARTERIAL LINE KIT- ICU, Pack Number ART245C Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits labeled as: 1) 3” RADIAL ARTERIAL LINE KIT- ICU, Pack Number ART240B Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits labeled as: UMBILICAL VESSEL TRAY, Pack Number UVT1100 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits labeled as: 1) BONE MARROW TRAY, Pack Number SPEC0255 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits, labeled as: 1) BREAST BIOPSY KIT, Pack Number MNS6950A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure kits, labeled as: 1) ARTHROGRAM TRAY, Pack Number DYNDH1349 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, labeled as: 1) BIOPSY TRAY-LF, Pack Number SPEC4380 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: 1) NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack… Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAPH TRAY, Pack Name MNS12670A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAM, Pack Number DYNDH1446A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: 1) CIRCUMCISION TRAY, Pack Number CIT6860A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: SHAVE KIT, Pack Number MNS8250 Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAM TRAY, Pack Number MNS11965A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Centurion procedure packs, containing Caina syringes, labeled as: 1) BREAST BIOPSY KIT, Pack Number DYNDH1512A Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNo state named
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Data in RES. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. Class IIFDA’s classSep 4, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 4, 2024ClassClass IIStatusOngoingWhereNationwide
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.”
Your shortlist0 of 4
Add one more to compare.