Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 2554125560 of 29,286 recalls

Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: MOST Options" System (MOST) HINGED TIB INS SZ 1 16MM Recalled by Zimmer,...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT Recalled...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II Unicompartmental Knee System: UNI ALL-POLY TIB SZ 1-7mm...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II Constrained Knee System NKII CCK TIB INS SZ00/0-L Recalled...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 Recalled by...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II System ULTRA CONG INS LT SZA/9MM ULTRA CONG Recalled by...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· Allesee Orthodontic Appliances

Recalled Item: AOA Distalizer Lock Nut Screw Recalled by Allesee Orthodontic Appliances Due...

The Issue: The Lock Nut component of the Jet appliances may be missing the screw...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: R Recalled by DePuy Orthopaedics, Inc. Due to DePuy Orthopaedics has...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RS-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L Recalled by DePuy Orthopaedics, Inc. Due to DePuy Orthopaedics has...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: R S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· Nico Corp.

Recalled Item: Myriad handpiece Tissue morcellator Recalled by Nico Corp. Due to This...

The Issue: This recall has been initiated due to a defective component within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2014· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) LIMB HOLDERS Recalled by DeRoyal Industries Inc Due to Moldy...

The Issue: Moldy smell in product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2014· Medical Information Technology, Inc.

Recalled Item: MEDITECH Microbiology Recalled by Medical Information Technology, Inc. Due...

The Issue: Potential for erroneous result reporting.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS TT4 Calibrator For the quantitative measurement of total thyroxine...

The Issue: Total T4 Calibrators and Reagent Packs may have calibration failures or low...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2014· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter...

The Issue: Biosense Webster is recalling the PentaRay Nav Catheter because it has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing