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 27812800 of 30,686 recalls

Medical DeviceOctober 22, 2024· Carwild Corporation

Recalled Item: Ivalon Eye Wick 20cm- Intended to be used for the Recalled by Carwild...

The Issue: Potential for package seal to be out of specification and the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2024· Carwild Corporation

Recalled Item: Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic...

The Issue: Potential for package seal to be out of specification and the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Biomet, Inc.

Recalled Item: JuggerLoc/ToggleLoc 2.9mm Drill Guide Recalled by Biomet, Inc. Due to Firm...

The Issue: Firm received complaints reporting that guides were warped when pulled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Karl Storz Endoscopy

Recalled Item: Irrigation Tubing for KARL STORZ Endomat Select UP210 Recalled by Karl Storz...

The Issue: Due to improper labeling of products. An intended use on the label has not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Iris Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Tip protector may fall off within the packaging, resulting in compromised...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain...

The Issue: A manufacturing defect causes Atellica CH Reaction Ring Cuvette Segments...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica¿ CH ¿2-Microglobulin (B2M) - In vitro diagnostic use in Recalled by...

The Issue: Potential for falsely depressed auto-diluted results for samples above the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 18, 2024· HUMAN MED AG

Recalled Item: human med Biofill Infiltration Cannula Recalled by HUMAN MED AG Due to The...

The Issue: The cannula tubes do not comply with the specification. The water jet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2024· LivaNova Deutschland GmbH

Recalled Item: Essenz HLM (Heart-Lung Machine) Recalled by LivaNova Deutschland GmbH Due to...

The Issue: Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2024· Roche Diagnostics Operations, Inc.

Recalled Item: cobas HCYS Recalled by Roche Diagnostics Operations, Inc. Due to Abnormal...

The Issue: Abnormal calibration signals and control recovery issues on the Homocysteine...

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

Class II — Potential Health HazardOngoing