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 30481–30500 of 55,837 recalls
Recalled Item: NICU ECC Pack BEQ-TOP 39202 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory Recalled by Datascope Corporation Due to...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22702 ECC W/HMOD 30000 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 25500 ECC 3/8 w/QiD Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Patient ECC Pack BEQ-TOP 22301 Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECC Small - Respiratory BEQ-TOP 5210 Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-T 9410 Lurie Chldns Small 1/4 Recalled by Datascope Corporation Due to...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 24500 ADULT ECC Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-TOP 13901 RAPID RESPONSE Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bliss anti-stress formula Dietary Supplement Recalled by Market America Inc...
The Issue: Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...
The Issue: Teleflex is recalling these products because the jaws of the tool tip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Multi Lumen CVC Kit (Central venous catheter) Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.