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. 1,906 recalls have been distributed to Minnesota in the last 12 months.
Showing 24681–24700 of 52,120 recalls
Recalled Item: da Vinci SP Instrument Arm Drape. QTY 1 Pouch Recalled by Intuitive...
The Issue: The instrument drape may tear while draping the Patient Side Cart presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.) Recalled by The...
The Issue: A stray strand of stainless-steel cable may protrude from the heat shrink...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...
The Issue: Potential metal burrs in the holes of the device preventing the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets Recalled by...
The Issue: Labeling: Incorrect Instructions; Instructions included for use with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets Recalled by...
The Issue: Labeling: Incorrect Instructions; Instructions included for use with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Catapres .2 (clonidine hydrochloride Recalled by Boehringer Ingelheim...
The Issue: Failed Dissolution Specifications: OOS resultsduring routine stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Recalled...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 128 Multi-slice CT Scanner System Product Usage: The Multi-Slice...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more...
The Issue: False resistant results for Streptococcus anginosus and Streptococcus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage:...
The Issue: Inspection process at the manufacturer found nonwoven material was used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Smooth Guide Wire - Bullet Tip Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Trypticase Soy Agar with 5% Sheep Blood Recalled by Becton Dickinson...
The Issue: a portion of a single lot was not manufactured in accordance with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...
The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.