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. 2,480 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,480 in last 12 months

Showing 4322143240 of 53,342 recalls

DrugOctober 16, 2014· Hospira Inc.

Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: A returned customer sample was evaluated and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 16, 2014· Pharmaceutical Associates Inc

Recalled Item: Cyproheptadine HCl Syrup (Cyproheptadine HCl Oral Solution Recalled by...

The Issue: Failed Impurities/Degradation Specifications : Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 16, 2014· Skeletal Dynamics

Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...

The Issue: Report received where the Align Radial Stem fractured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2014· Materialise USA LLC

Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...

The Issue: The box of guides for a specific case arrived intact but contained two (2)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
FoodOctober 15, 2014· U.B.C Food Distributors, LLC

Recalled Item: Mango flavored gelatin mix desert Recalled by U.B.C Food Distributors, LLC...

The Issue: Voluntary recall of strawberry flavored gelatin mix and mango flavored...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2014· U.B.C Food Distributors, LLC

Recalled Item: Strawberry flavored gelatin mix desert Recalled by U.B.C Food Distributors,...

The Issue: Voluntary recall of strawberry flavored gelatin mix and mango flavored...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2014· AMS Health Sciences

Recalled Item: Saba Shark Cartilage Complex Dietary Supplement Recalled by AMS Health...

The Issue: The product is being recalled due to the potential presence of Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 15, 2014· American Medical Systems, Inc.

Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...

The Issue: During routine periodic packaging testing, AMS identified that in simulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2014· American Medical Systems, Inc.

Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...

The Issue: During routine periodic packaging testing, AMS identified that in simulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2014· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...

The Issue: Issuing a device correction because if the pin bushing is over loaded or...

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

Class II — Potential Health HazardOngoing
DrugOctober 14, 2014· Hospira Inc.

Recalled Item: 5% Dextrose and 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...

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

Class II — Potential Health HazardOngoing
Refund