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. 2,768 recalls have been distributed to Florida in the last 12 months.
Showing 18481–18500 of 30,686 recalls
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Right Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...
The Issue: The software is not identifying the patient as having atypical hyperplasia,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...
The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...
The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (20 ml Size) Recalled by Instrumentation Laboratory Co....
The Issue: Instrumentation Laboratory Co. received customer reports of performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Firebird NXG Spinal Fixation System Decorticating Planer Recalled by...
The Issue: The plastic core of the Decorticating Planer was found to be missing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel Recalled by...
The Issue: Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JANUS & JANUS G3 Automated Workstation is an automated programmable Recalled...
The Issue: We have become aware through internal testing that JANUS and Janus G3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Saver Elite Processing Kit Recalled by Haemonetics Corporation Due to...
The Issue: Haemonetics has received isolated reports that in some cases the 70ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.