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. 2,627 recalls have been distributed to Michigan in the last 12 months.
Showing 19541–19560 of 53,342 recalls
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Microvel Double Velour Vascular Graft...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oryx Cervical Screw Caddy Recalled by Innovasis, Inc Due to Cervical screw...
The Issue: Cervical screw caddies have incorrect text markings for the 4.5mm Fixed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Augomation System using the Aliquoter Module (Inpeco P/N FLX-212)...
The Issue: Potential for discrepant patient results due to a potential for the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION IMPACT 10CC and OSTEOVATION Recalled by Skeletal Kinetics, Llc...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUMED IMPACT 10CC. Product Number: 65-0110-S Recalled by Skeletal Kinetics,...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION RMX 5CC. Product Number: 390-6001 Recalled by Skeletal Kinetics,...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION EX Recalled by Skeletal Kinetics, Llc Due to Bone void filler...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.