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. 1,132 recalls have been distributed to Florida in the last 12 months.
Showing 13521–13540 of 55,837 recalls
Recalled Item: SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market Recalled...
The Issue: Firm received 10 complaints of skin barrier delamination issues (e.g. flange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 Recalled by Smith &...
The Issue: Right nails were anodized, marked, and labelled as left nails and vice versa
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Synergy Washer/Disinfector Recalled by Steris Corporation Due to...
The Issue: The firm identified that when the electrical contactor component in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 10 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 40 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 20 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Gel USP Recalled by McKesson Corporation dba McKesson...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halobetasol Propionate Ointment 0.05% Net Wt. Recalled by McKesson...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by McKesson Corporation dba...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Prilocaine Cream USP Recalled by McKesson Corporation dba McKesson...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rebel Pistachio Ice Cream Recalled by Rebel Creamery Due to Pistachio ice...
The Issue: Pistachio ice cream may contain pistachio nut shells.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oakworks Bed (Emergency Field Bed) Recalled by Oakworks Inc Due to The...
The Issue: The warning label was printed with the incorrect weight capacity. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PX200 Emergency Relief Bed Recalled by Oakworks Inc Due to Product label was...
The Issue: Product label was printed without the UDI number and warning label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Effluent Sample Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 Liters Drain Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Recalled by Baxter Healthcare Corporation Due to Certain Peritoneal...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Prong Manifold Set (with Luer Connectors) Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APD Drain Manifold Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Cap for PD Catheter Adapter Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.