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. 2,491 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,491 in last 12 months

Showing 1978119800 of 28,355 recalls

Medical DeviceJune 28, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess...

The Issue: It was reported that the specified lots of the 2.4mm Titanium Locking Screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe Recalled by ConMed...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Cardinal Health

Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to Recalled by Cardinal...

The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes...

The Issue: One lot of BD Trucount Absolute Counting Tubes (IVD) may not be sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Moller Vital

Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...

The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Baxter Healthcare Corp.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter is issuing a safety alert in response to postmarketing reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...

The Issue: A variation in flute depth on the routers was observed. The variation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· Cook Inc.

Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...

The Issue: Potential coating contamination with glass particles.

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

Class I — Serious Health HazardOngoing