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. 2,683 recalls have been distributed to Florida in the last 12 months.
Showing 36661–36680 of 55,837 recalls
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...
The Issue: A variation in flute depth on the routers was observed. The variation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...
The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter is issuing a safety alert in response to postmarketing reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...
The Issue: Potential coating contamination with glass particles.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...
The Issue: Superpotent drug: Out of specification test result for assay during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Figi's Gifts in Good Taste Recalled by Figi's, Inc Due to Potential Listeria...
The Issue: Figi's Companies, Inc is recalling 2 products that are related to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Snack Shoppe Recalled by Figi's, Inc Due to Potential Listeria Contamination
The Issue: Figi's Companies, Inc is recalling 2 products that are related to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nabisco Honey Maid Teddy Grahams Cinnamon Cubs Graham Snacks Net Recalled by...
The Issue: Teddy Graham Cub Snacks were produced using Grain Craft Flour containing...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Michael's Naturopathic Programs Cholesterol Metabolism Factors 270 count...
The Issue: May contain undeclared milk (in the form of calcium caseinate) and soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to...
The Issue: Crystallization: Product contains particulate identified to be crystallized...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...
The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...
The Issue: Incorrect CO2 readings with some patient monitors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.