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. 1,822 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,822 in last 12 months

Showing 4374143760 of 55,837 recalls

DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Par Pharmaceutical Inc.

Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...

The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Apotex Inc.

Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to CGMP...

The Issue: CGMP Deviations: Product excipient was not re-tested at the appropriate date.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 11, 2015· Mylan Institutional LLC

Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL,...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 12x40 Airway Stent System Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Loading Unit w/ DST Series Technology 60mm - 3.5mm...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Silicone Round Drain Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - GIA Auto Suture Loading Unit w/ Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange FEMORAL CANAL TIP Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange PhysioMesh Flexible Composite Mesh 10cm x 15cm...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange X-SAW BLADE Recalled by EXP Pharmaceutical Services...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange BAG Recalled by EXP Pharmaceutical Services Corp Due...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange -APPLIER Recalled by EXP Pharmaceutical Services...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· DePuy Orthopaedics, Inc.

Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...

The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Dilating Tip Trocar w/Stability Sleeve 11mm...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Surgical Gown - Flyte Hood Pouch Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing