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. 2,698 recalls have been distributed to Minnesota in the last 12 months.
Showing 421–440 of 52,120 recalls
Recalled Item: VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 Recalled by Canon Medical System,...
The Issue: There is a potential for formation of ice occurring in the venting system of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsator Arterial Blood Sampling Kit Recalled by ICU Medical Inc. Due to...
The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 Recalled by Canon Medical System,...
The Issue: There is a potential for formation of ice occurring in the venting system of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...
The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL Recalled by Imprimis NJOF, LLC Due to...
The Issue: Presence of particulate matter - Glass like particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Moxifloxacin Ketorolac Recalled by Imprimis NJOF, LLC Due to...
The Issue: Presence of particulate matter - Glass like particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Moxifloxacin Recalled by Imprimis NJOF, LLC Due to Presence of...
The Issue: Presence of particulate matter - Glass like particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...
The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baraka French Style Puff Pastry 1lb and 1.5lbs sizes Recalled by ZIYAD...
The Issue: May contain partially hydrogenated oils
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baraka Gourmet Pastry Kunafe 6.7oz. Recalled by ZIYAD BROTHERS IMPORTING Due...
The Issue: May contain partially hydrogenated oils
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG) Recalled by...
The Issue: Lack of Assurance of Sterlity
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AlternatiV+ Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Push-In Suture Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixone Biocomposite Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixone Hybrid Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlternatiV+ Max Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.