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. 2,706 recalls have been distributed to Florida in the last 12 months.
Showing 30641–30660 of 30,686 recalls
Recalled Item: 4.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitrack System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...
The Issue: Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. Recalled by...
The Issue: GE initiated a correction to the instructions/use due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory...
The Issue: Distribution of a product that did not meet specifications. (labeling error)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Precision MPi is an all-digital multipurpose tilt-C x-ray system Recalled...
The Issue: It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.