Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,057 recalls have been distributed to Michigan in the last 12 months.
Showing 16421–16440 of 53,342 recalls
Recalled Item: Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX PLUS Analyzer with E3800 PC units. The Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illuminated Stepped Laser Probe Curved-for use in combination with 23G...
The Issue: Barcode label extended expiration date. Barcode located at the short side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended...
The Issue: Cooling Unit (CLU) expelled out of a CT gantry of an iCT system may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betadine (Povidone-Iodine) 5% Recalled by Edge Pharma, LLC Due to Defective...
The Issue: Defective container; syringe content migrating past the seal of the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 15 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 30 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO AB Recalled by DJ Orthopedics de Mexico S.A. de C.V....
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI RDS VENOUS STENT System Product Usage: is indicated for Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY PRO Recalled by DJ Orthopedics de Mexico S.A. de C.V. Due to failed...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI VENOUS STENT System Product Usage: is intended for the Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...
The Issue: The firm was notified by an ingredient supplier of Medium Chain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...
The Issue: The firm was notified by its ingredient supplier of Medium Chain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hostesss SnoBalls packaged as Hostess Chocolate CupCakes Recalled by HOSTESS...
The Issue: SnoBalls snack cakes were packaged with a label for Chocolate CupCakes...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kit: Injection REVIEW MAI Kit Part Number: 74736 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture. MAI Kit Part Number: 80315D Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT CHEST TUBE TRAY. Medical convenience kit Recalled by Avid Medical,...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture MAI Kit Part Number: 80076 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.