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. 2,911 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,911 in last 12 months

Showing 58615880 of 30,686 recalls

Medical DeviceAugust 22, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...

The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2023· Carl Zeiss Suzhou Co., Ltd.

Recalled Item: OPMI LUMERA 300 Recalled by Carl Zeiss Suzhou Co., Ltd. Due to Surgical...

The Issue: Surgical microscope for use in ophthalmology may be missing a screw from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedBank MedPass Software Recalled by CareFusion 303, Inc. Due to...

The Issue: After dispensing a timed dose medication for a patient, the automated...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2023· Impedimed Limited

Recalled Item: SOZO Bilateral Arm L-Dex Software Recalled by Impedimed Limited Due to...

The Issue: Bilateral L-Dex assessment software does not have the same level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2023· Exocad GmbH

Recalled Item: exoplan version 3.1 Rijeka Software -A medical software Recalled by Exocad...

The Issue: A software library filtering error has been discovered which occurs when...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2023· Philips North America Llc

Recalled Item: Patient Information Center iX with Software Version Number 4.x in Recalled...

The Issue: Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA Recalled by Smiths Medical ASD...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PNVMNIB21 Recalled by Cardinal...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Portacath Pack Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing