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. 2,698 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,698 in last 12 months

Showing 3336133380 of 55,837 recalls

Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Parker Laboratories, Inc.

Recalled Item: Sterile Aquasonic 100 Ultrasound Transmission Gel Recalled by Parker...

The Issue: There is a potential for the gel packets to have leaks in the packet seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· CardioTek BV

Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...

The Issue: Software bug which allows parameters to be changed unintentionally during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...

The Issue: An unexpected transient mode switch behavior was detected by Medtronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...

The Issue: An extremely dusty computer can cause problems at system start, or rarely,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Datascope Corporation

Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...

The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· XTANT MEDICAL INC

Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...

The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Medica Corporation

Recalled Item: EasyCAL HbA1c Calibrator Recalled by Medica Corporation Due to Patient...

The Issue: Patient results determined using this calibrator lot might deviate up to...

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

Class II — Potential Health HazardOngoing
FoodApril 11, 2017· Jimmy's Cookies

Recalled Item: The Bakery Peanut Butter Chocolate Chunk Cookies Recalled by Jimmy's Cookies...

The Issue: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 10, 2017· Vertical Pharmaceuticals, Inc.

Recalled Item: Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin Recalled...

The Issue: One (1) lot (21511158) of the OB Complete DHA is being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 10, 2017· Quaker Oats Co

Recalled Item: Tropicana 100% JUICE Recalled by Quaker Oats Co Due to One lot of Tropicana...

The Issue: One lot of Tropicana orange juice, may have small plastic fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 10, 2017· CooperSurgical, Inc.

Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...

The Issue: The current secondary packaging, a box, incorrectly states that the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· bioMerieux, Inc.

Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...

The Issue: Some anomalies have been identified during manufacturing controls.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· Ion Beam Applications S.A.

Recalled Item: Proton therapy system -Proteus 235 aka Proteus Plus. A medical Recalled by...

The Issue: A PBS (Pencil Beam Scanning) irradiation may pause for different reasons....

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

Class II — Potential Health HazardOngoing