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. 2,824 recalls have been distributed to Florida in the last 12 months.
Showing 16581–16600 of 55,837 recalls
Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...
The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to The polyester-based...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP A 40 Recalled by Philips Respironics, Inc. Due to The...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP Hybrid A30 (not marketed in US) Recalled by Philips...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut R Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO PLUS Delivery Catheter System Recalled by Medtronic...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solifenacin Succinate Tablets Recalled by CIPLA Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arjo Citadel beds originally assembled with the IndiGo modules during...
The Issue: The IndiGo power cord might wear during use which could lead to its damage,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for 15%...
The Issue: There is a potential for 15% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D Imaging Recalled by GE OEC Medical Systems, Inc Due to There is a...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Recalled by...
The Issue: Due to a design issue, inflation syringe handle separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite mobile C-arm - Product Usage: intended to provide Recalled by GE...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lingen SAMPLE Disposable Virus Sampling Kit pack Recalled by Mercedes...
The Issue: No 510(k) clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lingen Disposable Virus Sampling Kit Recalled by Mercedes Medical, Inc. Due...
The Issue: No 510(k) clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.