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. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 25701–25720 of 29,186 recalls
Recalled Item: G2001: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043G-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...
The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1469J: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System....
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M ESPE Imprint II Regular Body Recalled by 3M Company - Health Care...
The Issue: Specific lots of Imprint II and Paradigm impression material packs are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normative Data Template CD for use with the I-Portal devices. Used to...
The Issue: The data provided on the Normative Data Template CD for use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA N Control Recalled by Horiba Instruments, Inc dba Horiba Medical...
The Issue: Horiba Medical is recalling the ABX PENTRA N Control because it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Veris MR Monitor units The system is intended to Recalled by Medrad...
The Issue: The main board, P/N 301641, installed in some Medrad Veris MR Monitor units...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled by Steris...
The Issue: Customers indicated fluctuations in environmental conditions sites and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Propaq LT Series monitors. Model numbers 802LTAN Recalled by Welch Allyn...
The Issue: Welch Allyn will update Propaq 802 Series Vital Signs Monitor, models are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...
The Issue: Individual discs in the lot may not be sufficiently impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.