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. 2,530 recalls have been distributed to Minnesota in the last 12 months.
Showing 18361–18380 of 29,186 recalls
Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NMT Patient Cable (989803174581) in use with lntelliVue NMT Module Recalled...
The Issue: Manufacturing defect may cause localized heating, 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: 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: 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. 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: 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: 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: 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: 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: 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: 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: Willscher Vas Skewers Recalled by Cook Inc. Due to COOK Medical is...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartMonitor 2 PS/PSL Recalled by Circadiance LLC Due to Circadiance has...
The Issue: Circadiance has determined that it is possible for certain Smart Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.