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. 1,819 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,819 in last 12 months

Showing 5060150620 of 55,837 recalls

Medical DeviceJuly 15, 2013· China Daheng Group Inc.

Recalled Item: Denlase: Diode Laser Therapy System and Penlase: Dental Laser Therapy...

The Issue: Failure to provide calibration procedures to purchasers, as required by 21...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (100 Count Retail Canada)Catalog Number:...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (10 Count Canada)Catalog Number: 43877 Recalled...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
FoodJuly 15, 2013· Greenland Trading Corp

Recalled Item: El Basham Weight 400 g Ingredients: Natural Apricot Juice Recalled by...

The Issue: Kamar Deen AL Basham Apricot Dried Paste does not declare product identity...

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

Class III — Low RiskOngoing
Refund
FoodJuly 12, 2013· High Quality Organics, Inc.

Recalled Item: Dried Oregano Recalled by High Quality Organics, Inc. Due to Potential...

The Issue: High Quality Organics was notified by a customer who received a lot of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.75% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.25% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular Recalled...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Ormco/Sybronendo

Recalled Item: Brand Name: Vector TAS 8mm Screw. The Device Listing Number Recalled by...

The Issue: Ormco Corporation is voluntarily recalling one lot of 8 MM Vector TAS Screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Custom Medical Specialties, Inc.

Recalled Item: 5 x 93 US Probe Cover CMS-6049 Recalled by Custom Medical Specialties, Inc....

The Issue: No endotoxin (LAL) testing to proper level.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Celera Corporation

Recalled Item: OLA Buffer For Laboratory Use Recalled by Celera Corporation Due to The...

The Issue: The package insert for FG OLA Buffer, GPR displayed the wrong concentration...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoGel AIR 84 Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: Complaints were received from the field indicating that some Air Pumps were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VS Grafts >or= 6mm Intended for use in arterial vascular...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VXT Vascular Grafts >or= 6mm Intended for use in Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Bifurcated Grafts >or= 6mm Intended for use in Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene Trumpet Grafts >or= 6mm Flixene GW and GWT Grafts Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene IFG with Assisted Delivery Intended for use in arterial Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing