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. 1,823 recalls have been distributed to Minnesota in the last 12 months.
Showing 40361–40380 of 52,120 recalls
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium Injection USP Recalled by Pharmedium Services, LLC Due to...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Terra Spice Company barbeque spice blend (dry spice mix) Recalled by...
The Issue: Greenies, LLC dba Terra Spice Co. decided to conduct a voluntary recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terra Spice Company the Greek (dry spice mix) Recalled by Greenies LLC...
The Issue: Greenies, LLC dba Terra Spice Co. decided to conduct a voluntary recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terra Spice Company Jalapeno Cheddar (dry spice mix). Sold in 0.5 Recalled...
The Issue: Greenies, LLC dba Terra Spice Co. decided to conduct a voluntary recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terra Spice Company buffalo wing rub (dry spice mix). Sold in 0.5 Recalled...
The Issue: Greenies, LLC dba Terra Spice Co. decided to conduct a voluntary recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terra Spice Company Italian Seasoning w/ romano (dry spice mix) Recalled by...
The Issue: Greenies, LLC dba Terra Spice Co. decided to conduct a voluntary recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terra Spice Company basil walnut pesto blend (dry spice mix) Recalled by...
The Issue: Greenies, LLC dba Terra Spice Co. decided to conduct a voluntary recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil Recalled by Stroheckers Inc...
The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule...
The Issue: Marketed without an approved NDA/ANDA: The distributed units of Monistat 1...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...
The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...
The Issue: Some rods may not meet the appropriate traceability requirements including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...
The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...
The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.