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. 2,728 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,728 in last 12 months

Showing 2386123880 of 55,837 recalls

DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Lidocaine 0.5%/Phenylephrine 0.75% P.F. INJ Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Dexamethasone Sodium Phosphate Preservative Free Sterile Solution for INJ...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Isoproterenol HCL in D5W Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Isoproterenol HCL in D5W (Sterile to Sterile) Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Riboflavin 5-Phosphate Sodium Ophthalmic Solution Recalled by Premier...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Mitomycin Preservative Free Irrigation Recalled by Premier Pharmacy Labs Inc...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Isoproterenol HCL in D5W (Non Sterile to Sterile) Recalled by Premier...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Orphenadrine Citrate Sterile Injectable Solution *Contains Sulfites*...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Phenylephrine HCL PF INJ in 0.9% Sodium Chloride Recalled by Premier...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Sodium Bicarbonate INJ 8.4% Recalled by Premier Pharmacy Labs Inc Due to...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...

The Issue: Supplemental information provided with devices indicates that the subdural...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...

The Issue: The products' cut, coagulate, or blend function may not operate with the use...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...

The Issue: Supplemental information provided with devices may indicate that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Epimed International, Inc.

Recalled Item: Versa - Kath Mini Kit Recalled by Epimed International, Inc. Due to Mislabeling

The Issue: Mislabeled - The product's labeling contains an incorrect size for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Depth Electrodes Recalled by Ad-Tech Medical Instrument Corporation Due to...

The Issue: Supplemental information provided with devices indicates that the subdural...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Howmedica Osteonics Corp.

Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...

The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Epimed International, Inc.

Recalled Item: Versa - Kath Mini Kit Recalled by Epimed International, Inc. Due to Mislabeling

The Issue: Mislabeled - The product's labeling contains an incorrect size for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...

The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...

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

Class II — Potential Health HazardOngoing
FoodJune 18, 2019· Mott's LLP

Recalled Item: Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Recalled by...

The Issue: Elevated levels of inorganic arsenic

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

Class III — Low RiskOngoing
Refund