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 43981–44000 of 53,342 recalls
Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...
The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to There is a possibility the handle...
The Issue: There is a possibility the handle of the laryngoscope may heat up and melt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.0 MM TI Cannulated Screw Instrument and Implant Set Recalled by...
The Issue: A screw set was returned from the field for destruction after being exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...
The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...
The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens has become aware of the potential malfunction when using syngo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...
The Issue: STERIS has identified that deformation of the washers door handle pin may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...
The Issue: The Life Force chamber is marketed and promoted as a medical device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...
The Issue: The following defects have been identified for data loaded with Patient Data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...
The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...
The Issue: CGMP Deviations: These products are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...
The Issue: CGMP Deviations: These products are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LORTUSS EX Recalled by Poly Pharmaceuticals, Inc Due to Does Not Meet...
The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POLY-TUSSIN AC LIQUID Recalled by Poly Pharmaceuticals, Inc Due to Does Not...
The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TranSmart Raspberry Filled frozen unbaked cookie dough Recalled by CSM...
The Issue: Undeclared Allergen; Peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...
The Issue: The attachment latch mechanism can become bent depending on user handling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...
The Issue: Using the PA230E transducer with a user-defined setting with the output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G.A.C. 375 Injection USP Recalled by Medical Supply Liquidators Llc Due to...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.