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. 1,823 recalls have been distributed to Minnesota in the last 12 months.
Showing 40581–40600 of 52,120 recalls
Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...
The Issue: Multiaxial screws may not meet internal requirements related to fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinnamon Almonds Recalled by Trader Joes Company Due to Undeclared Peanuts
The Issue: Trader Joes Company is recalling its 16 ounce packages of Trader Joes...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BADIA Ground Cumin Recalled by Badia Spices, Inc. Due to Undeclared Peanut
The Issue: Undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Captopril Tablets Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: out of specification for thickness.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S IRRIGATION Recalled by Hospira Inc. Due to Non-Sterility:...
The Issue: Non-Sterility: Confirmed customer report of dark, fibrous particulates...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INFX-8000V Interventional Angiography System. CAT-880B catheterization...
The Issue: The table base rotational brake that holds the table top may not always be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO Recalled by Philips...
The Issue: The firm was notified by a customer that the collimator exchange carriage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Persona¿ Anterior Sizer with Locking Boom The Recalled by...
The Issue: Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Sizer with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.