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. 2,517 recalls have been distributed to Michigan in the last 12 months.
Showing 35541–35560 of 53,342 recalls
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfacetamide Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...
The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE) Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE)- Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...
The Issue: In some cases it has been difficult or not possible to disassemble the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE)-1st Generation Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard with Compressor ventilator Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA GDE upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due to...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.