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. 2,615 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,615 in last 12 months

Showing 4658146600 of 55,837 recalls

Medical DeviceJune 15, 2014· McKesson Technologies, Inc.

Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...

The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2014· Vita Food Products, Inc.

Recalled Item: Vita Classic Premium Sliced Smoked Atlantic Nova Salmon Recalled by Vita...

The Issue: This voluntary recall is being initiated due to a positive Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 13, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...

The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
DrugJune 12, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...

The Issue: Failed Dissolution Specifications: Stability results found the product did...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2014· Thorne Research Inc

Recalled Item: Captomer-250 [succinic acid (from 250 mg DMSA)] capsules Recalled by Thorne...

The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2014· Thorne Research Inc

Recalled Item: Captomer [succinic acid (from 100 mg DMSA)] capsules Recalled by Thorne...

The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2014· Biolase Technology Inc

Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...

The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Heartsine Technologies, Limited

Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...

The Issue: A small number of sealed foil pouches containing the electrodes were found...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Pentax Medical Company

Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...

The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Zimmer Manufacturing B.V.

Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...

The Issue: Two lots of screws were commingled. Screws with etching and machining for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Suture Set Recalled by Medical Action Industries Inc Due to Some of the...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Safety Laceration Kit Recalled by Medical Action Industries Inc Due to Some...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Max Barrier Kit Recalled by Medical Action Industries Inc Due to Some of the...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Laceration/Suture Removal Recalled by Medical Action Industries Inc Due to...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Laceration Trays Recalled by Medical Action Industries Inc Due to Some of...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Laceration Kit: W/Needles Recalled by Medical Action Industries Inc Due to...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing