Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,138 recalls have been distributed to Florida in the last 12 months.
Showing 12521–12540 of 30,686 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: 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: Aptio Automation System using the Aliquoter Module (Inpeco P/N FLX-212)...
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: 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: 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: Inpeco FlexLab Recalled by Inpeco S.A. Due to When analyzer sample carousel...
The Issue: When analyzer sample carousel lid remains open or manual process is too...
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: 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: EXACTECH OSSILIX FORM (MX) 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: 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: SKAFFOLD 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: CRANIOSCULPT C 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: OSTEOVATIONEX 2CC INJECT FORMULA. Product Number: 390-0002 Recalled by...
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 C 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 C 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 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: EXACTECH OSSILIX MP FIL 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: MEDTRONIC BONE VOID FILLER 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: 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: 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.