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 2598126000 of 28,355 recalls

Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL Anaerobe CNA Agar with 5% Sheep Blood // Recalled by Becton Dickinson...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin (KV)...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Carestream Health, Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-ray System. Produces radiographic images....

The Issue: Carestream Health Inc. is recalling the power plug on their DRX-Revolution...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2013· Becton Dickinson & Co.

Recalled Item: BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV Recalled by Becton...

The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2013· Synthes USA HQ, Inc.

Recalled Item: 5.0mm Unit Rod 270mm 5.0mm Unit Rod 290mm 5.0mm Unit Recalled by Synthes USA...

The Issue: DePuy Synthes has issued a Medical Device Correction notice for the 5.0mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Aristos MX Solid State Flat Panel Digital Imager Recalled by Siemens...

The Issue: Siemens issued a Field Safety Notice about the potential hazard to patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2013· Fisher Scientific Co

Recalled Item: Fisherbrand Sterile Swab Recalled by Fisher Scientific Co Due to The firm is...

The Issue: The firm is recalling Fisherbrand Sterile Swabs due to 4 customer complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) Mass Creatine Kinase MB Isozyme Calibrator (RC420) The Mass...

The Issue: Siemens Healthcare Diagnostics has received complaints that the lyophilized...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Utah Medical Products, Inc

Recalled Item: Deltran Disposable Pressure Transducer Kit (DPT Kit) Extracorporeal...

The Issue: Utah Medical Products, Inc. is recalling certain Deltran Disposable Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Baxa Corporation

Recalled Item: ExactaMix 1200 and 2400 Compounders. Used as an automated pumping Recalled...

The Issue: Baxter Healthcare is recalling certain ExactaMix automated compounding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Mesa Laboratories, Inc., Bozeman Manufacturing Facility

Recalled Item: Mesa Smart-Read EZTEST BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for...

The Issue: Self-contained steam biological indicator, are recalled because Mesa...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Cardiovascular Custom Cardiovascular Procedure Kits containing an...

The Issue: Over-Pressure Safety Valves not cleared with an indication for use on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Invacare Corporation

Recalled Item: Invacare Power Wheelchair Recalled by Invacare Corporation Due to Unintended...

The Issue: Unintended slowing or deceleration, and on rare occasion, unanticipated and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2013· Respironics California Inc

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California Inc Due to...

The Issue: Respironics California, Inc. has initiated a recall on the V60 ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 4, 2013· Mesa Laboratories, Inc., Bozeman Manufacturing Facility

Recalled Item: Mesa EZtest BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for use in...

The Issue: Mesa EZTest , Self-contained steam biological indicator, are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Intrathecal Catheter Pump Segment Revision Kit Recalled by...

The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic is providing Healthcare Professionals with important safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic INDURA 1P Intrathecal Catheter Recalled by Medtronic...

The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2013· Integra LifeSciences Corp.

Recalled Item: CMC Saddle Product Usage: The Ascension CMC is intended to Recalled by...

The Issue: As a result of a quality review, labelling content discrepancies were...

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

Class III — Low RiskOngoing
Medical DeviceJune 3, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX Evolution System Recalled by Carestream Health Inc. Due to...

The Issue: Due to potential for an x-ray exposure technique change.

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

Class II — Potential Health HazardOngoing