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. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 1801–1820 of 29,186 recalls
Recalled Item: REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487...
The Issue: Due to a software issue, the software may incorrectly process the date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artix MT Thrombectomy Device Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular software versions 6.x Recalled by Philips...
The Issue: An issue was identified with the software when using the Echo Module of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as...
The Issue: Disconnection of the adapter from the endotracheal tube can potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio 1 Granules for Filling ¿ 1 mm (2 cm¿) Recalled by SCIENCE & BIO...
The Issue: Vials of implant bone granules may contain less product then specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US...
The Issue: Incorrect labeling in which the front red pouch label did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray Platte Faxitron Recalled by Klinika Mdical Gmb Due to Potential...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray. KlinioTray. Tissue resection margin examination board/small....
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Recalled by Integra LifeSciences...
The Issue: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Preset treatment parameters are not consistently being used in accordance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...
The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...
The Issue: Devices for the affected lot were not assembled according to product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...
The Issue: Due to manufacturing issues, abutment products were manufactured with screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HistoCore PELORIS 3 Recalled by Leica Biosystems Melbourne Pty Ltd Due to...
The Issue: There is a leakage issue associated with the tubing in the manifold of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.