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. 2,654 recalls have been distributed to Minnesota in the last 12 months.
Showing 9161–9180 of 29,186 recalls
Recalled Item: SIGNA Pioneer nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR450w 1.5T nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system Recalled...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Creator Recalled by GE Healthcare, LLC Due to Under certain...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T nuclear magnetic resonance imaging system Recalled by...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Voyager nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Artist nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750 3.0T nuclear magnetic resonance imaging system Recalled by...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier nuclear magnetic resonance imaging system Recalled by GE...
The Issue: Under certain conditions, some slices may be missing which can lead to a gap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...
The Issue: The product package may potentially contain a mismatched graft that does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch Recalled by...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.