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. 2,590 recalls have been distributed to Arkansas in the last 12 months.
Showing 13821–13840 of 28,355 recalls
Recalled Item: Endotrac EPF/EGR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0:...
The Issue: There is a potential that the image of one patient could get unexpectedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR and Argyle acute hemodialysis catheters Recalled by COVIDIEN LLC...
The Issue: The priming volume values printed on the MAHURKA and Argyle acute catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliBridge System configured with a regional setting which uses...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center iX configured with a regional setting...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...
The Issue: The sensor's look up calibration files were incorrectly programmed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...
The Issue: The pressure gauge (manometer) may dislodge from the threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...
The Issue: There is an error in the chromomap on the package insert.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...
The Issue: There is the potential that a HeatWrap could include cells that have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...
The Issue: There is the potential that a HeatWrap could include cells that have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...
The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...
The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)...
The Issue: The bearings of the saw attachments were ungreased.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.7 Degree Straight Sagittal Saw attachment (Mako Total Knee Application...
The Issue: The bearings of the saw attachments were ungreased.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450A Recalled by Centurion Medical...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OR VANTEX 7FR 3L 16CM CVC ECVC6665 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.