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. 2,463 recalls have been distributed to Michigan in the last 12 months.
Showing 43641–43660 of 53,342 recalls
Recalled Item: Comfort Shield Barrier Cream Cloths with dimethicone a) 8 count NDC...
The Issue: Microbial Contamination of Non-Sterile Products: Comfort Shield Barrier...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chiclets Gum Recalled by Mondelez Global Llc Due to Undeclared Soy
The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Chiclets Peppermint Gum Recalled by Mondelez Global Llc Due to Undeclared Soy
The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chiclets Assorted Variety Multipak - Fruit Flavor Gum Recalled by Mondelez...
The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chiclets Gum Recalled by Mondelez Global Llc Due to Undeclared Soy
The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Chiclets Fruit Flavor Gum Recalled by Mondelez Global Llc Due to...
The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to Due to an anomaly in the...
The Issue: Due to an anomaly in the packaging process, it is possible that a defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Charnley PN Retract & Handle Recalled by DePuy Orthopaedics, Inc. Due to The...
The Issue: The small extraction peg of the Charnley Pin Retractor and Handle set is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology" Hemo intended for complete physiological/hemodynamic...
The Issue: Software Error: The McKesson Cardiology Hemo calculation section incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ysio Systems with software version VC10 The Ysio enables Recalled by...
The Issue: Siemens discovered that an unlikely error may occur on the Ysio system with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Medical Patient Monitor is a Physiological Recalled by Spacelabs...
The Issue: The clinician did not realize the monitor was in END CASE mode and was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...
The Issue: Sterility of device is not assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes Part number: 8900-4012...
The Issue: Sterility of device is not assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard DuaLok Breast Lesion Localization Wire Recalled by Bard Peripheral...
The Issue: Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes ((singles) Part...
The Issue: Sterility of device is not assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsule Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsule Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rx CHOICE brand LIQUID VITAMIN C Recalled by Hi-Tech Pharmacal Co., Inc. Due...
The Issue: The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Activia Lowfat Yogurt Blueberry 4 x 4oz Recalled by The Dannon Company, Inc...
The Issue: The recalled product includes an ingredient (condensed skim milk) that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...
The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.