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. 2,614 recalls have been distributed to Arkansas in the last 12 months.
Showing 11861–11880 of 49,990 recalls
Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...
The Issue: A forced shutdown of one of the processors did not generate a watch dog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...
The Issue: The instrument is incorrectly color coded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...
The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...
The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...
The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...
The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...
The Issue: An issue with propagation of treatment course information from RayStation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...
The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to The...
The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...
The Issue: SE primer may be missing some or all of the resin portion of the chemistry....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...
The Issue: The product was potentially exposed to below-recommended storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Software related alarm escalation defect occurs after approximately 25 days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GreenLight HPSEA Laser Fibers Recalled by Boston Scientific Corporation Due...
The Issue: Several complaints were received for the affected lot; users received a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...
The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...
The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Recalled by...
The Issue: Salmonella. Product made using recalled Jif peanut butter
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...
The Issue: Due to Titanium plasma coating not present implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.