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. 2,698 recalls have been distributed to Michigan in the last 12 months.
Showing 7421–7440 of 53,342 recalls
Recalled Item: SCORPIO TS TIB INSERT. Intended for knee replacement Part Number: 72-4-7518...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TS TIB INSERT -Intended for knee replacment Part Number: 72-4-7516...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LARGE PRIMARY REV.TIB.INSERT- DURACON Intended for knee replacement Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S Recalled by...
The Issue: Olympus identified inconsistencies in the Instructions for Use regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bkActiv Ultrasound System 2300 Recalled by B-K Medical A/S Due to An issue...
The Issue: An issue on the Dual Live Compare feature on the bkActiv system could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Link Patella Glide Resection Guide- For the implantation of the Recalled by...
The Issue: Mislabeled: Angle and height of the device marked as L(large) corresponds to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GammaPod - Treatment Planning System-a component of the GammaPod Irradiation...
The Issue: Wrong structures imported into the GammaPod Treatment Planning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Recalled by Philips North America Llc Due to Multiple...
The Issue: Multiple software issues that affect device functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM)...
The Issue: The software application on the Programmer/Recorder/Monitor (PRM) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod 5 App (on compatible Android smartphones) Recalled by Insulet...
The Issue: The bolus calculator is not recording the decimal point if it is the first...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 9251R1 Recalled by Busse Hospital Disposables, Inc. Due to Firm...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE Recalled by...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE Recalled by...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gaw's Deluxe Italian sub 12oz Recalled by Gaws Gourmet Foods Due to...
The Issue: undeclared sesame
Recommended Action: Do not consume. Return to store for a refund or discard.