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. 2,489 recalls have been distributed to Minnesota in the last 12 months.
Showing 24021–24040 of 29,186 recalls
Recalled Item: Nerve Block Tray (Nerve Block convenience kit) Recalled by Centurion Medical...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott m2000sp Recalled by Abbott Molecular Due to Some versions of...
The Issue: Some versions of Application Specifications (App Spec) are incompatible with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...
The Issue: Some of vials were found to be partially filled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Pneumo Groups 2-14 Latex Test Recalled by Remel Inc Due to...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucose Hexokinase (Liquid) Reagent For the in vitro quantitative...
The Issue: Product is not performing according to specifications. Control 2 does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Imaging Tray (General Surgery convenience kit) Recalled by...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) Recalled by...
The Issue: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JResultNet drivers using ASTM coding language. Calculator/data processing...
The Issue: Software issue resulting in the results of one patient potentially being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Expression MR200 MRI Patient Monitoring System. Recalled by Invivo...
The Issue: The MR 200 devices failed the initial power up test due to capacitor short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. and Recalled by...
The Issue: All packages of Falope Ring Band Applicator kits are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Introducer Kit Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Centesis Catheter Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by Radiometer America Inc Due to...
The Issue: Batches of HemoCue Glucose 201 Microcuvettes show discoloration and provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASEPT 2000 ml Drainage Bag Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE Calcitonin Control Module (IMMULITE Recalled by Siemens Healthcare...
The Issue: A typographical error regarding the expiration date was identified in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASEPT Peritoneal Drainage System Recalled by Pfm Medical Inc Due to PFM...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veta Peritoneal Catheter Kit Recalled by Pfm Medical Inc Due to PFM Medical...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.