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 13681–13700 of 30,686 recalls
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...
The Issue: Incomplete seal and premature expiration of individually packaged Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...
The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...
The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...
The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...
The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: There is a potential performance issue as detected by an under-recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: There is a potential performance issue as detected by an under-recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...
The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: There is a potential performance issue as detected by an under-recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...
The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI:...
The Issue: A portion of the lot was incorrectly packaged with a 12.5cm catheter instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...
The Issue: Potential for failure of the patient leakage current test. There is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...
The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceCure Cryoablation System ProSense -Intended for cryogenic destruction of...
The Issue: Updated User Manual DSR3200000 Rev. E to include the safety guidelines in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.