Medical devices, 2014
Shortlist up to four to read them side by side.
3,059 medical device recalls FDA’s Enforcement Report published in 2014, 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 7, 2026.
3,059of 3,059 medical device recallsshown with your filters
The list
- Medical device recall Magna-Fx Cannulated Screw Fixation System 7.0 mm Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall FREE-LOCK LAG SCREW, 12.7, FREE-LOCK LAG SCREW, 15.8, FREE-LOCK SUPRACOND TUBE and FREE-LOCK TUBE & SCP PLAT Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM, LAG SCR 12.7D X 55 MM SHO up to… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VERSA-FX II KEYLESS TUBE, VERSA-FX II KEYLESS SHORT, VERSA-FX II SHORT TUBE PL, VERSA-FX II STD TUBE PLAT and… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VERSA-FX KEYLESS 90D X 8 and X 11, VERSA-FX KEYLESS 95D X 8, X 11, and X 14, VERSA-FX KEYLESS 140D X 4 and X… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall M/DN R-F IM NAIL 9MM DIA , 10 MM, 11 MM, 12 MM, 13 MM and 14 MM Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall RECON SCREW LG 5.5MM DIA and M/DN FEM IM NAIL 8MM DIA to 16 MM DIA Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INTERLOCKING IM SCREW SML, MED and LRG Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some items starting with codes 0022530 Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall M/DN HUMERAL I/M NAIL Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ASIA ONE-PIECE LAG SCREW Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ITST ANTI-ROTATION SCREW and FEM IM NAIL Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ONE-PIECE LAG SCREW 11MM Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall DISTAL MEDIAL FEMORAL CON, DISTAL POSTERIOR/LATERAL, DISTAL SMALL VOLAR RADIUS, PROXIMAL DORSAL ULNA PLT, and… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MOORE HIP PROS LONG FENES, MOORE HIP PROS NRW STR FE, MOORE HIP PROS STR FENEST, THOMPSON HIP PROSTHESIS 3,… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MOORE HIP PROS LONG FENES, MOORE HIP PROS NRW STR FE, MOORE HIP PROS STR FENEST, THOMPSON HIP PROSTHESIS… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MODULAR AUSTIN MOORE FENE Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bipolar liners and Multipolar cups with the following dimensions in MM Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEXGEN OSTEOTOMY CORT BON Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEXGEN MIS TIBIA PLATE PR NEXGEN TAPER PLUG NEXGEN PRECOAT PEG TIB PL NEXGEN MICRO ALL-POLY PAT NEXGEN… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFFSET LI Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O TRILOGY ACET SHELL 40MM O TRILOGY ACET SHELL 42MM O… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HGP II ACETABULAR CUP BON Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HGP II ACETABULAR CUP MOD Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall PRESSFIT FEM ST FX 16 X 1 Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VERSYS HERITAGE FEM STEM Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 12/14 UNIPOLAR FEMORAL HE VERSYS CEM LD/FX SZ 11X12 VERSYS CEM LD/FX SZ 12X12 VERSYS CEM LD/FX SZ 14X13… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZIMTRON 6 DEG 22 HEADS Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 12/14 COCR FEMORAL HEAD Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CPT 12/14 COCR (various sizes) Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 6 DEGREE COCR FEM HEAD 36 Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes) Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall FEM HD ION (various sizes) Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HERBERT BONE SCREW, 3.0MM and HERBERT CANNULATED BONE S Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall COMPRESSION SCREW Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM PERI SCR. 3.5MM X 14MM PERI SCR 3.5MM X 44MM STE PERI SCR.… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA 2.7 X 8 CORT SCREW/SELFTA 2.7 X 9 CORT SCREW/SELFTA 2.7 X… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT SCREW HEX/SE 2.0 X 10 CORT SCREW CRUCI 2.0 X 12 CORT SCREW CRUCI 2.0 X… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 3.5 COMP PLT, 4 HOLE 3.5 COMP PLT, 5 HOLE 3.5 COMP PLT, 6 HOLE 3.5 COMP PLT, 8 HOLE 3.5 COMP PLT, 9 HOLE 3.5… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT SCREW SELFT 3.5 X 14 CORT SCREW SELFT 3.5 X 16 CORT SCREW SELFT 3.5 X… Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CartoUnivu Module Biosense Webster has initiated a recall of the CartoUnivu Module within the Carto 3 System (V3.2.2 and V3.2.3) when used with Siemens Axiom Artis VB… Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement Report5 statesnamed in where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereCalifornia, Kentucky, Massachusetts, New Jersey and Utah
- Medical device recall Synthes Driving Cap/Threaded Both parts are intended for use in the Tibia system, LFN and RAFN systems The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent Insertion Handles when assembled becoming difficult to separate. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall External Implant RBT, D3 Threadform 4.0 X 10.5mm The body length of the External Implant 40105D3 Lot 1302762 labeled as 10.5mm in length is in fact 12mm in length. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Illinois, Louisiana, North Carolina, New York and Pennsylvania named
- Medical device recall Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error… XVI can incorrectly calculate the target position of the treatment table. Class IIFDA’s classFeb 26, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 39 states named PublishedFeb 26, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Connecticut, District of Columbia, Florida, Georgia, Idaho, Illinois, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Dakota, Tennessee, Texas, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
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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