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. 2,716 recalls have been distributed to Michigan in the last 12 months.
Showing 5721–5740 of 29,286 recalls
Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box as labeled: Regard Recalled by CooperSurgical, Inc. Due to Incorrect...
The Issue: Incorrect component descriptions within the "Contents" section on the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates:...
The Issue: Potential for baseplate peripheral holes to be out of specification due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...
The Issue: Device is breaking while in use, potential for patients to require a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...
The Issue: There is the potential that the safety shield may not properly engage on IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...
The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...
The Issue: Various medical devices potentially exposed to rodent and rodent activity....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Full screen error message may occur on patient monitors with affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFS Flat screen support arm systems without surgical lamp for Recalled by...
The Issue: The stopper block on the LFS bracket could be broken or missing. Without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFS Flat screen arm system with surgical lamp for Models Aurora series...
The Issue: The stopper block on the LFS bracket could be broken or missing. Without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinchlock SS Knotless Anchor Inserter Recalled by Stryker Corporation Due to...
The Issue: Expired Product distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Knee insert...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apellis Injection Kit 29g Injection Needle -single use intended to Recalled...
The Issue: 19-gauge x 1" inch filter needles showed appearances of a small fraction of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett Cuff Pressure Manager Recalled by Covidien Due to Inadequate...
The Issue: Inadequate internal fixation of the power inlet port to the cuff pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used Recalled...
The Issue: Handbook Revision (Rev13) a dilution step is indicated as an Action when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm...
The Issue: Some catheter kits labeled as 23 cm implant length incorrectly included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.