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. 2,622 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,622 in last 12 months

Showing 4364143660 of 55,837 recalls

Medical DeviceMarch 2, 2015· Hill-Rom, Inc.

Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...

The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2015· Baxter Healthcare Corp

Recalled Item: Master Drug Library Software version 8.0 Recalled by Baxter Healthcare Corp...

The Issue: Loading/Bolus default dose settings in the Master Drug Library and the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2015· Akorn, Inc.

Recalled Item: Fluticasone Propionate Nasal Spray Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Stability Specifications: Out of specification for preservative,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodFebruary 27, 2015· Unilever United States, Inc.

Recalled Item: Talenti Gelato & Sorbetto Recalled by Unilever United States, Inc. Due to...

The Issue: Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Stryker received four customer complaints reporting that inside the box...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 26, 2015· Ethicon Endo-Surgery Inc

Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...

The Issue: During an internal inspection of the production process the firm discovered...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...

The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Quest Medical, Inc.

Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...

The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...

The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2015· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp....

The Issue: Nonapproved labeling claims (Sterile)

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2015· Captiva Spine, Inc

Recalled Item: Captiva's lumbar intervertebral fusion system Reamers (color code rings on...

The Issue: It is possible for the titanium color-coded ring to detach from the Reamers.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2015· Boston Scientific Corporation

Recalled Item: Various Lots of Expel Drainage Catheter with TwistLoc Hub Biliary Recalled...

The Issue: Complaints of device fragmentation after the catheter was implanted in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing