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. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 30941–30960 of 52,120 recalls
Recalled Item: SCHRITTMACHER ANGIO X3 Recalled by Medtronic Due to Potential for an...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM SUTURE PACK Recalled by Medtronic Due to Potential for an incomplete...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiLite Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Cook...
The Issue: Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT Recalled by Medtronic Due to...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practice Kit Recalled by Medtronic Due to Potential for an incomplete...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USPACK-SUTURE KIT Recalled by Medtronic Due to Potential for an incomplete...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH Recalled by Medtronic Due...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R Recalled by Medtronic Due to...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc....
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutty INFUSIONS Roasted Cashew Butter Recalled by HVF Inc. d.b.a Huson...
The Issue: Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nutty INFUSIONS Ginger Wasabi Cashew Butter Recalled by HVF Inc. d.b.a Huson...
The Issue: Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carestation 620 A1 Recalled by GE Healthcare, LLC Due to Carestation 620,...
The Issue: Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD Recalled by...
The Issue: Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 70 Ultrasound System Intended for use by trained personnel (doctor...
The Issue: The strength of the arm mounting mechanism was insufficient and had to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic...
The Issue: Failed Impurities/Degradation Specifications: stability testing results did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Protein Bar 14 bars/box Recalled by Herbalife International Of America Inc...
The Issue: Herbalife is recalling Protein Bar-Peanut Butter because it may contain a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Brain 3.0 Stereotaxic instrument Computer-assisted surgical device....
The Issue: Robot arm being sent to the wrong position
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device....
The Issue: Robot arm being sent to the wrong position
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APLIO 500 TUS-A500 diagnostic ultrasound system Recalled by Toshiba American...
The Issue: When Continuous Trace method is used as the tracing method on Spectral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.