Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,652 recalls have been distributed to Nevada in the last 12 months.
Showing 12001–12020 of 28,334 recalls
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: Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model:...
The Issue: If the shaft breaks due to material fatigue, the trauma arm can fall down...
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: Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N...
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 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- 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: Accelerator a3600 Automation System using the Aliquoter Module (Inpeco P/N...
The Issue: In certain firmware versions, in case a Clot Detection error (error code...
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: Aptio 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: 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: CRANIOSCULPT FLOW 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.
Recalled Item: ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S Recalled by Skeletal...
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.
Recalled Item: CRANIOSCULPT 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: SKAFFOLD RENU FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void...
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 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: CRANIOSCULPT 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: SKAFFOLD CMF IMPRESS (MP) Recalled by Skeletal Kinetics, Llc Due to Bone...
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: OSTEOVATIONEX 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.