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. 2,393 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,393 in last 12 months

Showing 4412144140 of 52,120 recalls

Medical DeviceApril 21, 2014· Bausch & Lomb Inc- Greenville Solutions Plant

Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...

The Issue: Out of specification results for one of the two disinfectants.

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2014· Hospira Inc.

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

The Issue: Presence of Particulate Matter: Confirmed customer complaint that orange and...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2014· Apotex Corp.

Recalled Item: Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due...

The Issue: Subpotent Drug: Out of specification (OOS) results at the 9 month...

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

Class III — Low RiskOngoing
Refund
FoodApril 18, 2014· French Broad Luscious Chocolates

Recalled Item: French Broad Chocolates Recalled by French Broad Luscious Chocolates Due to...

The Issue: Cacao moth in the almonds of the chocolate bar.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 18, 2014· Leica Microsystems, Inc.

Recalled Item: Thyroglobulin (1D4) is a mouse anti-human monoclonal antibody produced as...

The Issue: Bond Ready to Use Primary Antibody Thyroglobulin does not function as...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
DrugApril 17, 2014· Wockhardt Usa Inc.

Recalled Item: Wockhardt Metoprolol Succinate Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Product was out of specification (OOS) at...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Trigen Laboratories, Inc.

Recalled Item: Triveen - PRx RNF Capsules Recalled by Trigen Laboratories, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Label indicates that the product...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Cubist Pharmaceuticals, Inc.

Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter: Customer complaint stating that one vial...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 17, 2014· Teleflex Medical

Recalled Item: Hudson RCI Adult Universal Ventilator Circuit Recalled by Teleflex Medical...

The Issue: Product is being recalled due to complaints that the inspiratory and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Nanosphere, Inc.

Recalled Item: Verigene Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled by...

The Issue: Nanosphere has determined that a portion of BC-GN Test Cartridge Lot number...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Gen-Probe Inc

Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...

The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2014· Mckesson Medical Immaging

Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...

The Issue: High priority alert icon was not displayed in the Study List when there are...

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

Class II — Potential Health HazardOngoing
DrugApril 16, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg Recalled by Pfizer...

The Issue: Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 16, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...

The Issue: DePuy Synthes is initiating a recall of certain lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Sakura Finetek USA Inc

Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...

The Issue: This Lot has variations in melting temperature.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Maquet Medical Systems USA

Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...

The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· HeartWare Inc

Recalled Item: HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) -...

The Issue: Patients and caregivers are instructed that if a battery does not provide...

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

Class II — Potential Health HazardOngoing