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. 2,939 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,939 in last 12 months

Showing 28012820 of 55,837 recalls

Medical DeviceApril 24, 2025· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: ABBOTT DIAGNOSTICS ALINITY I ANTI-CCPS REAGENT. Recalled by Mckesson...

The Issue: transit delays of certain cold chain products due to severe thunderstorms...

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

Class II — Potential Health HazardOngoing
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Artificial Tears Ophthalmic Solution Recalled by BRS Analytical Services,...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Gel 1% Recalled by BRS Analytical...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Polyvinyl Alcohol Ophthalmic Solution 1.4% Recalled by BRS Analytical...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Lubricant Eye Drops Solution Recalled by BRS Analytical Services, LLC Due to...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% Recalled by BRS...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 23, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: A new motor/encoder and cable was introduced into instruments manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· VIRTUAL INCISION CORPORATION

Recalled Item: MIRA SURGICAL SYSTEM Recalled by VIRTUAL INCISION CORPORATION Due to The...

The Issue: The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Mozarc Medical US LLC

Recalled Item: Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque...

The Issue: Potential breach of sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Mozarc Medical US LLC

Recalled Item: Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack....

The Issue: Potential breach of sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: A new software update (v1.20) is introducing error codes for the Dxl 9000...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Mozarc Medical US LLC

Recalled Item: Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque...

The Issue: Potential breach of sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane...

The Issue: Potential breach of sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Mozarc Medical US LLC

Recalled Item: Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque...

The Issue: Potential breach of sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2025· Beckman Coulter Ireland, Inc.

Recalled Item: Apo B Reagent Recalled by Beckman Coulter Ireland, Inc. Due to The product...

The Issue: The product Value Assignment Sheet (VAS) is used in calibration of the...

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

Class III — Low RiskOngoing
DrugApril 22, 2025· RemedyRePack Inc.

Recalled Item: Clindamycin HCl Capsule Recalled by RemedyRePack Inc. Due to CGMP Deviations...

The Issue: CGMP Deviations - products manufactured in a shared facility with Ezetimibe...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 22, 2025· 3M Company

Recalled Item: 3M Ranger Irrigation Fluid Warming Set Recalled by 3M Company Due to Notice...

The Issue: Notice was issued to clarify flow rates related to the inlet fluid temperature.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Solos Recalled by ICU Medical, Inc. Due to Internal testing...

The Issue: Internal testing found that Plum Duo pumps with software version 1.1.1 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Duo Recalled by ICU Medical, Inc. Due to Internal testing...

The Issue: Internal testing found that Plum Duo pumps with software version 1.1.1 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI...

The Issue: Affected kits contain recalled Integra Lifesciences Codman Disposable...

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

Class I — Serious Health HazardOngoing