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 15561–15580 of 49,990 recalls
Recalled Item: Betadine (Povidone-Iodine) 5% Recalled by Edge Pharma, LLC Due to Defective...
The Issue: Defective container; syringe content migrating past the seal of the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...
The Issue: The firm was notified by an ingredient supplier of Medium Chain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...
The Issue: The firm was notified by its ingredient supplier of Medium Chain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VICI VENOUS STENT System Product Usage: is intended for the Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI RDS VENOUS STENT System Product Usage: is indicated for Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 30 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO AB Recalled by DJ Orthopedics de Mexico S.A. de C.V....
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY PRO Recalled by DJ Orthopedics de Mexico S.A. de C.V. Due to failed...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 15 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flurandrenolide Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PERLA TL Lateral Connector Open - Product Usage: intended to Recalled by...
The Issue: Due to external labelling error/mix-up. Affected product external labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA ON-OFF KIT. Medical convenience kit Recalled by Avid Medical, Inc....
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIALYSIS ACCESS Medical convenience kit Recalled by Avid Medical, Inc. Due...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 3T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Recalled by INNOVA...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT CHEST TUBE TRAY. Medical convenience kit Recalled by Avid Medical,...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 7T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 Recalled by...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.