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. 1,900 recalls have been distributed to Florida in the last 12 months.
Showing 33741–33760 of 55,837 recalls
Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...
The Issue: Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...
The Issue: Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...
The Issue: Potential contamination of product with E. coli O157.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...
The Issue: Potential contamination of product with E. coli O157.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dixie Diners' Club Carb Not Beanit Butter Recalled by The SoyNut Butter...
The Issue: Potential contamination of product with E. coli O157.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing, LLC Due to...
The Issue: The main vial label lists the incorrect part number, but the cap label is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics notified customers that errors were contained in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...
The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myelotec Video Guided Catheters Recalled by Myelotec, Inc. Due to...
The Issue: Obstructed/blocked port from defective VGC Access Port Body component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...
The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Inion GRT Tack Recalled by Inion Ltd. Due to Aluminum pouch seal was noticed...
The Issue: Aluminum pouch seal was noticed to be defective (slightly open).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parmesan Truffle Salt. The product is packaged in glass taster Recalled by...
The Issue: Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...
The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fem IM Nail 14mmdx50cm right Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 17x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx48cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx38cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.