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. 2,673 recalls have been distributed to Minnesota in the last 12 months.
Showing 5261–5280 of 52,120 recalls
Recalled Item: Budesonide Recalled by Medisca Inc. Due to CGMP Deviations and Presence of...
The Issue: CGMP Deviations and Presence of Particulate Matter: Glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infla-650 Herbal Dietary Supplement Recalled by Guru Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules Recalled...
The Issue: CGMP Deviations: Out of specification for dissolution
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blemfree All Day Lotion (salicylic acid 0.5% w/w) Recalled by Equibal Inc...
The Issue: CGMP Deviations: Manufactured without following Current Good Manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Amerisource Health...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartMate 3 System Controllers provided within the following HeartMate 3...
The Issue: Left ventricular assist system controller UI membrane/screen may lift along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...
The Issue: The tube may fall into the surgical site during the grasping process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiple Digital Analog Products labeled as: NobelBiocare...
The Issue: Due to a manufacturing issue, the product has a out of specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P Recalled by CareFusion 303, Inc. Due...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK MINI CR-4HH-P Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.