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 14681–14700 of 49,990 recalls
Recalled Item: Aspirated Cyto-Histological Biopsy needle Recalled by M.D.L. S.r.l. Due to...
The Issue: Sterility assurance may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A303416A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone Marrow Transplantation biopsy needle Recalled by M.D.L. S.r.l. Due to...
The Issue: Sterility assurance may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A319516AM Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT...
The Issue: Firm's submission for Emergency Use Authorization (EUA) contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A399400A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A300316A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A902416 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSORB PLUS PREFILLED G-CAN 1.0L Recalled by Armstrong Medical Services...
The Issue: Some devices may be associated with high and unexpected resistance to gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOLLY & ME PECANS all natural PRALINE PECANS Recalled by Molly and Me Pecans...
The Issue: The firm was notified during an inspection by the State that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...
The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...
The Issue: Customers have reported an increased number of false positive SARS-CoV-2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by The Harvard Drug Group Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution Recalled by Teligent Pharma, Inc....
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...
The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...
The Issue: There is potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.