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. 2,710 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,710 in last 12 months

Showing 2978129800 of 55,837 recalls

Medical DeviceJanuary 5, 2018· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Recalled by...

The Issue: Contains a gel-like contaminant that may affect product performance.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2018· Toshiba American Medical Systems Inc

Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...

The Issue: The power supply unit may be damaged and may fail to start up when the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...

The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2018· International Laboratories, LLC

Recalled Item: Clopidogrel Tablets Recalled by International Laboratories, LLC Due to...

The Issue: LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2018· Dollar General Corporation, Inc.

Recalled Item: Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT...

The Issue: The firm received Ice Oatmeal Cookies that actually contain Coconut Macaroon...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2018· Ventura Foods Llc

Recalled Item: SunGlow Recalled by Ventura Foods Llc Due to Undeclared Soy

The Issue: SunGlow contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2018· Ventura Foods Llc

Recalled Item: SunGlow Recalled by Ventura Foods Llc Due to Undeclared Soy

The Issue: SunGlow contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 3, 2018· Holsum Baking Company Warehouse

Recalled Item: Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth...

The Issue: Firm was notified of a positive test result for Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: RASPBERRY Cream Ice Cream Bars: Sundae SHOPPE Recalled by Fieldbrook Foods...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Orange Cream Ice Cream Bars sold under the following labels: Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Chocolate Covered Vanilla Ice Cream Bars packaged under the following...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Ice Cream Variety Packs containing Sandwiches Recalled by Fieldbrook Foods...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· GETINGE US SALES LLC

Recalled Item: HEMASHIELD Knitted Double Velour Cardiovascular Fabric Recalled by GETINGE...

The Issue: A probable mislabeling of the product: a different-sized product is on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Ultrasound System Recalled by ESAOTE S.P.A. Due to The ultrasound...

The Issue: The ultrasound system used in certain settings may result in overheating of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Ultrasound System Recalled by ESAOTE S.P.A. Due to The ultrasound...

The Issue: The ultrasound system used in certain settings may result in overheating of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Teleflex Medical

Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...

The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...

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

Class II — Potential Health HazardOngoing