Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 982 recalls have been distributed to Minnesota in the last 12 months.
Showing 42581–42600 of 52,120 recalls
Recalled Item: Total Temporomandibular Joint Replacement System- 55mm Rt Standard Ti Mand...
The Issue: Laser etching on the parts is wider and deeper than the conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling:...
The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
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.
Recalled Item: MicroVue Bb Plus EIA is packaged as a kit which Recalled by Diagnostic...
The Issue: Samples are quantitating incorrectly, with approximately 50% higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: AlignRT- Intended for prescription use. The system is indicated for Recalled...
The Issue: Potential failure of AlignRT to assert interlock.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.