Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

30751–30775 of 40449

ModerateFDA (Devices)·Z-1125-2016·2016-03-23
Zimmer Manufacturing Recalls Distal Femoral Components Due to Calibration Data Issues
Zimmer Manufacturing B.V. is recalling 945 units of distal femoral components due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 27 consists of all product under product code: HSB and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON 234703206 DISTAL MEDIAL FEMORAL CON 234703208 DISTAL MEDIAL FEMORAL CON 234800504 DISTAL POSTERIOR/LATERAL 234800506 DISTAL POSTERIOR/LATERAL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1095-2016·2016-03-23
Pro-Dex Recalls Battery Packs for Surgical Screwdriver Due to Particulates
Pro-Dex Inc is recalling 1,995 sterile battery packs for the KLS Martin Max Driver because they may contain particulates within the sterile package.
Product
Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1170-2016·2016-03-23
Zimmer Zimtron Hip Arthroplasty Heads Recalled for Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 226 sterile Zimtron hip arthroplasty heads due to insufficient sealer calibration data. The affected units were packaged between August 2010 and April 2013.
Product
Product 72 consists of all product code: JDI and same usage: Item no: 805002202 ZIMTRON HEAD 12/14 0X22 MM For use in total or hemi hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2016·2016-03-23
Zimmer Manufacturing Recalls Mini Magna-FX Cann Screws Due to Calibration Data Issues
Zimmer Manufacturing B.V. is recalling 3,190 units of Mini Magna-FX Cann Screws because of insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 46 consists of all product under product code: HWC and same usage: Item no: 114204012 MINI MAGNA-FX CANN SCREW 114204016 MINI MAGNA-FX CANN SCREW 114204020 MINI MAGNA-FX CANN SCREW 114204024 MINI MAGNA-FX CANN SCREW 114204028 MINI MAGNA-FX CANN SCREW 114204032…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1143-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Knee Arthroplasty Bone Screws
Zimmer Manufacturing B.V. is recalling 3,696 sterile MGII Knee Self-Tap Bone Screws due to insufficient sealer calibration data.
Product
Product 45 consists of all product under product code: JWH and same usage: Item no: 511007020 MGII KNEE SLF-TAP BONE ST 511007025 MGII KNEE SLF-TAP BONE ST 511007030 MGII KNEE SLF-TAP BONE ST 511007035 MGII KNEE SLF-TAP BONE ST 511007040 MGII KNEE SLF-TAP BONE ST…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1116-2016·2016-03-23
Zimmer Manufacturing Recalls 83 Sterile Bone Fixation Screws
Zimmer Manufacturing B.V. is recalling 83 sterile bone fixation screws due to insufficient sealer calibration data. The products were distributed nationwide in the US.
Product
Product 18 consists of all product under product code: HWC and same usage: Item no: 47248001441 CANC SCR 4.0MM X 14MM FUL 47248001641 CANC SCR 4.0MM X 16MM FUL 47248001840 CANC SCR 4.0MM X 18MM 47248001841 CANC SCR 4.0MM X 18MM FUL 47248002041 CANC SCR 4.0MM X 20MM FUL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1097-2016·2016-03-23
Collagen Matrix Recalls NuOss XC Sinus Dental Grafts for Shelf Life Failure
Collagen Matrix Inc is recalling 347 units of NuOss XC Sinus dental grafts distributed in Massachusetts because some products failed to expand properly during shelf life testing.
Product
NuOss XC Sinus Reference No 509-3001 (BMCU17, size 17 mm diameter x 10 mm height) Reference No 509-3002 (BMCU22, size 22 mm diameter x 12 m height) Manufacturer:- Collagen Matrix, Distributor:- ACE Surgical Supply Co, Inc, Intended use for dental surgery such as…
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1117-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Hip Arthroplasty Stems Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling sterile cemented femoral stems for hip arthroplasty due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 19 consists of all product code: JDI and same usage: Item no: 765301101 CEM FEM ST 11X120 NOCOAT 765301201 CEM FEM ST 12X125 NOCOAT 765301301 CEM FEM ST 13X130 NOCOAT 765301401 CEM FEM ST 14X135 NOCOAT 765301501 CEM FEM ST 15X140 NOCOAT 765301601 CEM FEM ST…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1158-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Intramedullary Fixation Rods Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling 1,394 sterile intramedullary fixation rods and reconstruction screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 60 consists of all product under product code: HSB and same usage: Item no: 225207055 RECON SCREW LG 5.5MM DIA 225207555 RECON SCREW LG 5.5MM DIA 225208055 RECON SCREW LG 5.5MM DIA 225208555 RECON SCREW LG 5.5MM DIA 225209055 RECON SCREW LG 5.5MM DIA 225209555…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1111-2016·2016-03-23
Zimmer Manufacturing Recalls 34 Sterile Bone Fixation Screws
Zimmer Manufacturing B.V. is recalling 34 sterile bone fixation screws due to insufficient sealer calibration data. The affected units were packaged between August 2010 and April 2013.
Product
Product 13 consists of all product under product code HWC , and same usage: Item no: 47486510002 6.5 X 100 CANC SCREW, 32M Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1124-2016·2016-03-23
Zimmer Distal Femoral Components Recalled for Sterility Concerns
Zimmer Manufacturing B.V. is recalling specific distal femoral components used in hip arthroplasty due to insufficient sealer calibration data.
Product
Product 26 consists of all product under product code: JWH and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON 234703206 DISTAL MEDIAL FEMORAL CON 234703208 DISTAL MEDIAL FEMORAL CON 234800504 DISTAL POSTERIOR/LATERAL 234800506 DISTAL POSTERIOR/LATERAL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1109-2016·2016-03-23
Zimmer Manufacturing Recalls Hip Arthroplasty Femoral Heads Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling 366 units of 6 Degree COCR Femoral Heads used in hip arthroplasty due to insufficient sealer calibration data.
Product
Product 11 consists of all product under product code JDI , and same usage: Item no: 902602500 6 DEGREE COCR FEM HEAD 26 902602600 6 DEGREE COCR FEM HEAD 26 902602700 6 DEGREE COCR FEM HEAD 26 902602800 6 DEGREE COCR FEM HEAD 28 902602900 6 DEGREE COCR FEM HEAD 28…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1146-2016·2016-03-23
Zimmer NexGen All-Poly Patella Recalled for Sterility Concerns
Zimmer Manufacturing B.V. is recalling NexGen All-Poly Patella implants due to insufficient sealer calibration data affecting sterility.
Product
Product 48 consists of all product under product code: JWH and same usage: Item no: 597206526 NEXGEN ALL-POLY PATELLA, for use in total knee arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1114-2016·2016-03-23
Zimmer Manufacturing Recalls Bipolar Hip Liners Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 8,773 units of bipolar liners and shells for hip arthroplasty due to insufficient sealer calibration data.
Product
Product 16 consists of all product under poduct code: KWY and same usage: Item no: 500103822 BIPOLAR LINER 38MM OD X 2 500103922 BIPOLAR LINER 39MM OD X 2 500104022 BIPOLAR LINER 40/41MM OD 500104026 BIPOLAR LINER 40MM OD X 2 500104222 BIPOLAR LINER 42/43 OD X 500104226…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1183-2016·2016-03-23
Siemens Syngo Dynamics PACS Software Recall for Measurement Package Issue
Siemens is recalling Syngo Dynamics PACS software due to a potential issue in the VA10 measurement package. 228 units are affected nationwide.
Product
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637, 10091673 intended for acceptance, transfer, display, storage, archive acceptance, transfer, display, storage, archive and manipulation of digital medical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1106-2016·2016-03-23
Zimmer Manufacturing Recalls 3.5mm Cortical Screws Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 99 units of 3.5mm cortical screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 8 consists of all products under product code HWC, and same usage: Item no: 47483501201 3.5MM CORT. SCREW 12MM LN 47483501401 3.5MM CORT. SCREW 14MM LN 47483501601 3.5MM CORT. SCREW 16MM LN 47483501801 3.5MM CORT. SCREW 18MM LN 47483503601 3.5MM CORT. SCREW 36MM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1119-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Bone Fixation Appliances Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling 1,209 units of sterile metallic bone fixation appliances due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 21 consists of all product under product code: JDI and same usage: Item no: 811400218 CPT 12/14 COCR REVISION S 811400318 CPT 12/14 COCR REVISION S 811400420 CPT 12/14 COCR REVISION S 811400423 CPT 12/14 COCR REVISION S 811400426 CPT 12/14 COCR REVISION S…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1108-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Bone Fixation Screws Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling specific lots of sterile 4.5 x 26 Cortical Screws due to insufficient sealer calibration data during packaging.
Product
Product 10consists of all product under product code HWC, and same usage: Item no: 47484502601 4.5 X 26 CORT SCREW SELF Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1142-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Orthopedic Screws Due to Calibration Data Issues
Zimmer Manufacturing B.V. is recalling 4,335 sterile orthopedic screws and bone staples due to insufficient sealer calibration data.
Product
Product 44 consists of all product under product code: HWC and same usage: Item no: 114607099 MAGMA-FX CANN SCREW 7.0MM 114604099 MAGNA FX CANN SCREW 7.0MM 114603000 MAGNA-FX CANN SCREW 7.0MM 114603500 MAGNA-FX CANN SCREW 7.0MM 114604000 MAGNA-FX CANN SCREW 7.0MM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1136-2016·2016-03-23
Zimmer Manufacturing Recalls Interlocking Intramedullary Screws Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 4,752 sterile interlocking intramedullary screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 38 consists of all product under product code: HSB and same usage: Item no: 225303255 INTERLOCKING IM SCREW LG 225303555 INTERLOCKING IM SCREW LG 225303755 INTERLOCKING IM SCREW LG 225307055 INTERLOCKING IM SCREW LG 225302742 INTERLOCKING IM SCREW MED 225303242…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1168-2016·2016-03-23
Zimmer Versys Heritage Femoral Stem Recall Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling 360 units of Versys Heritage Femoral Stems due to insufficient sealer calibration data. The affected sterile products were packaged between August 2010 and April 2013.
Product
Product 70 consists of all product under product code: JDI and same usage: Item no: 785701000 VERSYS HERITAGE FEM STEM 785701100 VERSYS HERITAGE FEM STEM 785701200 VERSYS HERITAGE FEM STEM 785701300 VERSYS HERITAGE FEM STEM 785701320 VERSYS HERITAGE FEM STEM 785701400…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1096-2016·2016-03-23
Collagen Matrix Recalls NuOSS Cancellous Dental Product Due to Size Error
Collagen Matrix Inc is recalling 171 units of NuOSS Cancellous dental product shipped to Massachusetts because some units may have the incorrect size.
Product
NuOSS Cancellous Intended for use in dental surgery.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1157-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Polyethylene Patches Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling sterile polyethylene patches due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 59 consists of all product under product code: JWH and same usage: Item no: 42540000026 PSN ALL POLY PAT PLY 26MM 42540000029 PSN ALL POLY PAT PLY 29MM 42540000032 PSN ALL POLY PAT PLY 32MM 42540000035 PSN ALL POLY PAT PLY 35MM 42540000038 PSN ALL POLY PAT PLY…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1145-2016·2016-03-23
Zimmer Modular Hip Cups Recalled for Insufficient Sealer Calibration Data
Zimmer Manufacturing B.V. is recalling sterile modular hip cups due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 47 consists of all product under product code: LPH and same usage: Item no: 611004022 MODULAR CUP 10 DEGREE LIN 611004428 MODULAR CUP 10 DEGREE LIN 611004628 MODULAR CUP 10 DEGREE LIN 611004828 MODULAR CUP 10 DEGREE LIN 611004832 MODULAR CUP 10 DEGREE LIN…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1130-2016·2016-03-23
Zimmer Herbert Bone Screws Recalled for Insufficient Sealer Calibration Data
Zimmer Manufacturing B.V. is recalling 4,018 units of Herbert bone screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 32 consists of all product under product code: HWC and same usage: Item no: 47115401200 HERBERT BONE SCREW, 3.0MM 47115401400 HERBERT BONE SCREW, 3.0MM 47115401600 HERBERT BONE SCREW, 3.0MM 47115401800 HERBERT BONE SCREW, 3.0MM 47115402000 HERBERT BONE SCREW…
Category
Medical Device
Distribution
Distributed nationwide

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30751–30775 of 40449