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. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 441–460 of 52,120 recalls
Recalled Item: Genesis Dual Thread Screw-In 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.
Recalled Item: Genesis Screw-In 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: Qunol Recalled by QUTEN RESEARCH INSTITIUTE LLC Due to Mold contamination...
The Issue: Mold contamination detected for raw material lots that were produced in July...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...
The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...
The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical I2 Injection Kit Recalled by Vortex Surgical Inc. Due to...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 25GA I.D.D. Internal Delivery Device Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecfen Retractable Membrane Polisher Recalled by Vortex Surgical Inc. Due to...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical Lindsell Sutured IOL Marker Recalled by Vortex Surgical Inc....
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.