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. 2,706 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,706 in last 12 months

Showing 3142131440 of 55,837 recalls

DrugJune 28, 2017· GSK Consumer Healthcare

Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...

The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2017· Cardinal Health 200, LLC

Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...

The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Cardinal Health 200, LLC

Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...

The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Hologic, Inc

Recalled Item: Tomcat Instrument Recalled by Hologic, Inc Due to A Tomcat Instrument...

The Issue: A Tomcat Instrument software anomaly that causes the pipettor arm to make...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
FoodJune 27, 2017· Peanut Butter holdings, LLC

Recalled Item: PB Crave Recalled by Peanut Butter holdings, LLC Due to Mislabeling

The Issue: Product mislabeled. "'Contains " allergen statement under the ingredient...

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

Class III — Low RiskOngoing
Refund
FoodJune 26, 2017· NatureBox, Inc.

Recalled Item: NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookies made with whole...

The Issue: One piece of a cashew was found during packing of Mini Crispy Snickerdoodle...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Beckman Coulter Inc.

Recalled Item: Coulter LH 750 Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Ameditech Inc

Recalled Item: Alere iScreen Dx Urine Drug Screen Card Recalled by Ameditech Inc Due to The...

The Issue: The kit box label incorrectly identifies PCP (instead of TCA) as one of the...

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

Class III — Low RiskOngoing