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. 2,537 recalls have been distributed to Michigan in the last 12 months.
Showing 26741–26760 of 53,342 recalls
Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...
The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JouJou's white large pita bread Recalled by Constantine's International...
The Issue: Failure to declare wheat on the labeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Platinium CRT-D 1711 DF-1 Recalled by Sorin CRM SAS Due to Hardware...
The Issue: Hardware configuration may lead to overconsumption, followed by loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sorin Platinium CRT-D 1741 DF-4 Recalled by Sorin CRM SAS Due to Hardware...
The Issue: Hardware configuration may lead to overconsumption, followed by loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...
The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPARKLING MANDARIN JUICE DRINK Recalled by Gourmet International Inc. Due to...
The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SPARKLING GRAPEFRUIT JUICE DRINK Recalled by Gourmet International Inc. Due...
The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.