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. 1,113 recalls have been distributed to Michigan in the last 12 months.
Showing 2401–2420 of 29,286 recalls
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Continu-Flo Solution Set with Duo-Vent Spike Recalled by Baxter...
The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...
The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: The VITROS 5600 Integrated System software versions 3.8.0 may not correctly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...
The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bodor P and C series laser cutting machines Recalled by Jinan Bodor Cnc...
The Issue: Non-compliant laser products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...
The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.