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. 2,616 recalls have been distributed to Florida in the last 12 months.
Showing 44761–44780 of 55,837 recalls
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...
The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...
The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: Device may malfunction, which could cause therapy to be delayed, disabled,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx...
The Issue: KCI has received reports that, in a small number of cases, the CelluTome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and...
The Issue: HORIBA Medical is informing all HORIBA Medical Lite DM customers using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product comes in as part of Fabulous Fudge Gift Box. Recalled by Tastefully...
The Issue: Tastefully Simple is recalling various lots of Cookie & Cream Fudge(Fabulous...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lemoncello Mascarpone Cake Recalled by Cheesecake Royale, Inc. Due to...
The Issue: Recalled product contains undeclared FD&C Yellow #5 and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Turtle Fudge Brownies Recalled by Cheesecake Royale, Inc. Due to Undeclared...
The Issue: Recalled product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rocky Road Brownies Recalled by Cheesecake Royale, Inc. Due to Undeclared Wheat
The Issue: Recalled product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CARROT CAKE Recalled by Cheesecake Royale, Inc. Due to Undeclared Walnuts
The Issue: Recalled product contains undeclared walnuts. Walnut is not listed on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Karlsburger Foods Low Sodium Taco Seasoning Recalled by Karlsburger Foods,...
The Issue: Taco Seasoning has an allergen of milk in the product that is not declared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Karlsburger Foods Taco Seasoning Recalled by Karlsburger Foods, Inc. Due to...
The Issue: Taco Seasoning has an allergen of milk in the product that is not declared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.