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. 2,507 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,507 in last 12 months

Showing 3672136740 of 53,342 recalls

FoodMarch 3, 2016· Clorox Co (The)

Recalled Item: Hidden Valley Original Ranch dressing Recalled by Clorox Co (The) Due to...

The Issue: Incorrect ingredient labels inadvertently put on some bottles of salad...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugMarch 3, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zoledronic Acid Injection Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility; defective seals where the metal silver ring...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Dynarex Corporation

Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...

The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Roche Molecular Systems, Inc.

Recalled Item: Hand-Held Scanner USB IT3800 For sample identification and tracking when...

The Issue: The hand-held barcode scanner model IT3800 used with the COBAS AmpliPrep...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Circulatory Technology Inc

Recalled Item: Bigger-Better-Bladder With 3/8" ID tubing Recalled by Circulatory Technology...

The Issue: The seal between the balloon and the housing may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· ArthroCare Corporation

Recalled Item: TOPAZ MicroDebrider 0.8 mm Recalled by ArthroCare Corporation Due to During...

The Issue: During functional testing of devices after real time aging, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity Gauze Sponges Recalled by Covidien LLC Due to Compromised sterility...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing