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 27201–27220 of 29,186 recalls
Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...
The Issue: Two unsealed pouches were found at an Edwards' distribution location in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...
The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...
The Issue: This recall is being initiated because the affected lots of this product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire Recalled by...
The Issue: Medtronic has identified an issue involving specific lot numbers of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Calibrator 2-pack Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Calibrator 6-pack Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Archer Super Stiff Guidewire 0.035 inch (0.89mm) Recalled by...
The Issue: Medtronic has identified an issue with a specific lot of the Archer 0.035...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...
The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...
The Issue: The firm received complaints for unintended movements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...
The Issue: Philips Healthcare received a report from the field stating when they viewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...
The Issue: GE Healthcare has become aware of a potential safety issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...
The Issue: GE Healthcare is aware of a potential safety issue with the use of GE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....
The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Perinatal and Centricity Intensive Care is intended to be...
The Issue: 1) Under rare network conditions, a Centricity Perinatal process may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood and Recalled by Becton...
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrimaConnex Tapered Implant TC Recalled by Keystone Dental Inc Due to...
The Issue: Mislabeled: Cover screw that was in the package was a WD cover screw and not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All OneTouch Verio IQ Blood Glucose Meters sold as: Verio Recalled by...
The Issue: The Verio IQ meter will shut off and revert to set up mode at glucose values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms....
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.