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. 1,166 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,166 in last 12 months

Showing 6641–6660 of 55,837 recalls

Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) KIT CANISTER Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) GYN CDS Recalled by...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2024· IntegraDose Compounding Services LLC

Recalled Item: fentaNYL Citrate 2 Recalled by IntegraDose Compounding Services LLC Due to...

The Issue: Lack of Assurance of Sterility: leaking bags

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2024· B. Braun Medical Inc

Recalled Item: Lactated Ringer's Injection USP Recalled by B. Braun Medical Inc Due to Lack...

The Issue: Lack of assurance of sterility: bags have the potential to leak..

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2024· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Film (nonoxynol-9 Recalled by Apothecus...

The Issue: cGMP Diviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 21, 2024· AMY'S KITCHEN INC.

Recalled Item: Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085 Recalled...

The Issue: L. mono contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Vancomycin Hydrochloride for Oral Solution Recalled by Amneal...

The Issue: Superpotent Drug: Due to overfilling of drug powder

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 21, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Rifampin Capsules USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2024· SonarMed Inc

Recalled Item: AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed...

The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2024· SonarMed Inc

Recalled Item: AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed...

The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2024· SonarMed Inc

Recalled Item: AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed...

The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models:...

The Issue: Coolant level in the cooling circuit drops below a certain level, this may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing