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. 2,673 recalls have been distributed to Minnesota in the last 12 months.
Showing 4541–4560 of 29,186 recalls
Recalled Item: QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There...
The Issue: There are two windows on the test device, the control line window and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neria Soft Infusion Set Recalled by Unomedical A/S Due to Specific lots of...
The Issue: Specific lots of Neria Soft Infusion Sets, which have been shipped into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bed Assist Bars Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline is recalling certain lots of our Adult Portable Bed Rails that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bed Assist Bars Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline is recalling certain lots of our Adult Portable Bed Rails that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface Recalled by Baxter Healthcare Corporation Due...
The Issue: Inconsistencies were identified with service records associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...
The Issue: There is a risk of mistreatment as irradiation is not prevented when some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ2 Connect MDx-IVD Designed to perform automated isolation and purification...
The Issue: Insufficient welding leads to the heater cable becoming brittle and present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...
The Issue: Customer complaints were received regarding falsely elevated results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...
The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide Handpiece Adaptor Sleeve 1 Recalled by X-NAV Technologies, LLC Due...
The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...
The Issue: Customer complaints were received regarding falsely elevated results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus...
The Issue: Due to increase in complaints for the KD-640L and KD-645L Triangle Tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus...
The Issue: Due to increase in complaints for the KD-640L and KD-645L Triangle Tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs...
The Issue: Potential for positively biased results due to signal reduction over shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.