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. 2,661 recalls have been distributed to Arkansas in the last 12 months.
Showing 2321–2340 of 28,355 recalls
Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E...
The Issue: It was identified internally that two commingle events occurred where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C...
The Issue: It was identified internally that two commingle events occurred where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VARIPULSE Bi-Directional Ablation Catheter . The Field Catheter is Recalled...
The Issue: Due to an observed trend of neurovascular events
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irix-A Integrated Lumbar Fusion System Recalled by XTANT Medical Holdings,...
The Issue: Certain implants in the Irix-A Lumbar Fusion System were distributed while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Socrates 38 Aspiration Catheter 127 cm length The Recalled by Scientia...
The Issue: Due to manufacturing non-conformance that resulted in channels in the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK...
The Issue: Due to devices being irradiated above the established specification which my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access PCT Reagent Pack Recalled by Beckman Coulter Inc. Due to Identified...
The Issue: Identified reagent lots are experiencing a high rate of calibration failures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Recalled...
The Issue: Disposable set may leak during priming from a female quick connector due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL Recalled...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alteon XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled by...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY Recalled by MEDLINE...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT Recalled...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeiMed NasoGel for DRY NOSES UDI-DI/code: 00705928045309 SKU...
The Issue: Due to nasal spray stability failure for bioburden.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.