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. 2,619 recalls have been distributed to Arkansas in the last 12 months.
Showing 10121–10140 of 28,355 recalls
Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...
The Issue: Discoloration and turbidity were present in the specified lots of STMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...
The Issue: Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...
The Issue: The mirror may become detached and fall from the unit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLEUR-EVAC Thoracic Catheters (CATHETER Recalled by TELEFLEX MEDICAL INC Due...
The Issue: Teleflex is recalling this product due to a lack of assurance of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...
The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...
The Issue: The tube holder can separate from the barrier that secures the device to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating Table System Recalled by Getinge Group Logistics America, LLC Due...
The Issue: There is a potential for hydraulic leakage at the inclination function to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...
The Issue: This Field Action is being conducted following identification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A Recalled by...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...
The Issue: Use of the kits after incorrect storage could lead to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.