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. 2,591 recalls have been distributed to Arkansas in the last 12 months.
Showing 14841–14860 of 49,990 recalls
Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick Recalled by...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Cleansing Scrub Swabstick (1's) Recalled by Professional...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Prep Pad Large Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Swabstick (3's) Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodine Prep Pad MEDIUM Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidone-Iodide Cleansing Scrub Swabstick (3's) Recalled by Professional...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDI Povidine Iodine Swabstick (1's) Recalled by Professional Disposables...
The Issue: SubPotent: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norton Arm Kit Recalled by Aspen Surgical Products, Inc. Due to Affected...
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jessie Sterile Arm Suspension Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marco Shoulder Stabilization Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The...
The Issue: The kit contains the wrong vial tray in the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hiland 100% Pure Apple Juice From Concentrate No Sugar Added Recalled by...
The Issue: Elevated levels of inorganic arsenic.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baxter prismaflex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PrismaFlex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD" Mouse IgG2a Isotype Control APC X39 ASR Recalled by Becton, Dickinson...
The Issue: Complaints have been received for performance issues related to high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ Ultrasound Systems Recalled by Philips Ultrasound Inc Due to Ultrasound...
The Issue: Ultrasound system control panel arm swivel lock could fail, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.