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. 2,677 recalls have been distributed to Minnesota in the last 12 months.
Showing 3941–3960 of 29,186 recalls
Recalled Item: VICRYL (polyglactin 910) Suture - Indicated for use in general Recalled by...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II (polydioxanone) Suture - Intended for use in general Recalled by...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...
The Issue: The wrong configuration of the blade was in the package. The bevel was on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...
The Issue: The wrong configuration of the blade was in the package. The bevel was on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...
The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kosmos on iOS impacting iOS Recalled by Echonous Inc Due to Ultrasound...
The Issue: Ultrasound system has a bug in affected iOS software, which after DICOM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...
The Issue: The adjustment ring on the device may become loose resulting in the wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...
The Issue: Some of the devices may function incorrectly resulting in no temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Simultaneous ECG measurements with multiple devices, including a manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK CE-IVD Recalled by Becton, Dickinson and Company,...
The Issue: Multitest with compromised raw material used to assess immune system status...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.