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. 2,615 recalls have been distributed to Florida in the last 12 months.
Showing 55401–55420 of 55,837 recalls
Recalled Item: The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to...
The Issue: The firm recalled the product because it may cure harder than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultra-Short Magnetic Resonance Imaging System Recalled by Toshiba...
The Issue: The firm recalled due to a potentail problem with the position of the hold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus Tibia Plateau (component of the Columbus REVISION Knee System)...
The Issue: During an internal quality inspection, the tibia plateau was found to be out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...
The Issue: Presence of Foreign Substance(s): There is a potential for foreign...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...
The Issue: Presence of Foreign Substance(s): There is a potential for foreign...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...
The Issue: A technical alarm may be generated on the FLOW-i system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER Recalled by Vital...
The Issue: The EnFlow Warmer Strap does not meet the requirements of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunny Boy Peanut Butter. Product is labeled in part: 6/5 Recalled by...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is 1 oz Peanut Butter. 1 oz pouch labeled Recalled by Sunshine...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunny Boy Low Sodium/ Low Salt Peanut Butter. Product is Recalled by...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is 2 oz Peanut Butter. 2 oz pouch labeled Recalled by Sunshine...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunny Boy NoSalt Peanut Butter. No label was provided by Recalled by...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product is 50 lb Bag Peanut Butter. Product Case is Recalled by Sunshine...
The Issue: On 02/17/2012 Sunshine Peanut Company initiated a recall of Sunny Boy and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Carescape Patient Data Module with v2.0 software used Recalled...
The Issue: GE Healthcare became aware of two issues with the Patient Data Module using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...
The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...
The Issue: Incorrect technique applied may cause potential rupture of the tibialis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.