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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 26441–26460 of 30,686 recalls
Recalled Item: HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) -...
The Issue: Patients and caregivers are instructed that if a battery does not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...
The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...
The Issue: Test Strips may report an inaccurately low INR result. Several patients had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...
The Issue: When using a specific plan update workflow in combination with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...
The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...
The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...
The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...
The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...
The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...
The Issue: A stock check revealed broken glass fibers between the connector and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Luminos dRFsystem The Axiom Luminos dRF is intended to Recalled by...
The Issue: It was determined that under rare environmental conditions (i.e., extremely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in...
The Issue: Software anomaly: potential for delay in the reporting of patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.