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. 1,075 recalls have been distributed to Minnesota in the last 12 months.
Showing 16481–16500 of 52,120 recalls
Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LogiCal Monitoring Set Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific lots of...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tubing with male luer lock adapter (Component) a. 76 cm Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palm Cups - Product Usage: intended to be used to Recalled by Smiths Medical...
The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...
The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...
The Issue: Software is given wrong results going out to HIS on test that had reruns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...
The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Krazy Night capsule Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shogun-X capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triple SupremeZen Gold 3500 Recalled by Na Na Collection Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Platinum 5000 Recalled by Na Na Collection Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs up 7 Red 70K capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: foamyiQ Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%) Recalled...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Stability Specifications: product did not meet viscosity results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy E2 Sanitizing Handwash (Benzalkonium Chloride Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antiseptic Hand Cleaner (Chloroxylenol Recalled by Spartan Chemical Co Inc...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%)...
The Issue: Microbial Contamination of Non-Sterile Products; lot tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.