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. 1,749 recalls have been distributed to Minnesota in the last 12 months.
Showing 46041–46060 of 52,120 recalls
Recalled Item: Nature's Way Recalled by Schwabe North America, Inc. Due to Nature's Way...
The Issue: Nature's Way (NW) is voluntary recalling a number of products because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tacrolimus Capsules Recalled by Sandoz Incorporated Due to Cross...
The Issue: Cross Contamination with Other Products: findings of carryover of trace...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...
The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...
The Issue: A Hand Piece high deployment force exceeded the maximum specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreaCore¿ software. Versions subject to the limitation: 6.0 Recalled by...
The Issue: Vital Images, Inc. has found an issue in VitreaCore software though internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Empirical Labs Building Health Digesti-Zyme Recalled by Empirical...
The Issue: Empirical Labs is recalling certain lots of dietary supplements due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: All-Natural Greens Dietary Supplement Recalled by Empirical Laboratories,...
The Issue: Empirical Labs is recalling certain lots of dietary supplements due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Empirical Labs Building Health SuperFuel Tropical Dietary Supplement...
The Issue: Empirical Labs is recalling certain lots of dietary supplements due to...
Recommended Action: Do not consume. Return to store for a refund or discard.