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. 2,768 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,768 in last 12 months

Showing 1956119580 of 55,837 recalls

DrugJuly 21, 2020· Ferring Pharmaceuticals Inc

Recalled Item: STIMATE (desmopressin acetate) Nasal Spray1.5 mg/mL Recalled by Ferring...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2020· Ferring Pharmaceuticals Inc

Recalled Item: Desmopressin Acetate Nasal Spray 10 mcg/0.1 mL Recalled by Ferring...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2020· Ferring Pharmaceuticals Inc

Recalled Item: DDAVP Nasal Spray (desmopressin acetate) 10 mcg/0.1 mL Recalled by Ferring...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Mibelas 24 Fe (norethindrone acetate and ethinyl estradiol tablets and...

The Issue: Failed Impurities/Degradation Specifications: Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2020· BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

Recalled Item: Ezycare Face Mask Recalled by BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA...

The Issue: Disposable face masks labeled as non-medical were distributed to customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-CH EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Recalled by...

The Issue: May have one or more dimensional features out of tolerance includes: thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame Recalled by...

The Issue: Modular Junction Box (MJB) cables can melt and affect the bed functionality.

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

Class II — Potential Health HazardOngoing
DrugJuly 20, 2020· Liq-E S.A. De C.V.

Recalled Item: OPTIMUS LUBRICANTS Instant Hand Sanitizer Recalled by Liq-E S.A. De C.V. Due...

The Issue: Chemical Contamination: Products contain methanol and were below the label...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 20, 2020· Liq-E S.A. De C.V.

Recalled Item: OPTIMUS LUBRICANTS Instant Hand Sanitizer Recalled by Liq-E S.A. De C.V. Due...

The Issue: Chemical Contamination: Products contain methanol and were below the label...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 20, 2020· Liq-E S.A. De C.V.

Recalled Item: OPTIMUS LUBRICANTS Instant Hand Sanitizer Recalled by Liq-E S.A. De C.V. Due...

The Issue: Chemical Contamination: Products contain methanol and were below the label...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 20, 2020· Liq-E S.A. De C.V.

Recalled Item: OPTIMUS LUBRICANTS Instant Hand Sanitizer Recalled by Liq-E S.A. De C.V. Due...

The Issue: Chemical Contamination: Products contain methanol and were below the label...

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

Class I — Serious Health HazardOngoing
Refund