Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,451 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,451 in last 12 months

Showing 2570125720 of 28,355 recalls

Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count International 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 Plus Monitor System (Kit w/10 Count Vials Canada) Recalled by Nova...

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 Plus Monitor System (Kit w/10 Count Vials International) 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
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
Medical DeviceJuly 15, 2013· HemoCue AB

Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by HemoCue AB Due to During a...

The Issue: During a complaint investigation HemoCue AB discovered punctured HemoCue...

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 (10 Count Vials) Catalog Number: Recalled by...

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 (50 Count DME) Catalog Number: Recalled by Nova...

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 (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 Boxed) Catalog Number: Recalled by...

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 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· 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: Flixene IFG 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: 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 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: 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: Advanta SST Grafts >or= 6mm Intended for use in arterial 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 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· 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: Advanta VS 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 SuperSoft Grafts >or= 6mm 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