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. 2,645 recalls have been distributed to Arkansas in the last 12 months.
Showing 4041–4060 of 28,355 recalls
Recalled Item: Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Recalled by Centers For Disease Control and Prevention Due to The H5b...
The Issue: The H5b component may fail to amplify, resulting in an inconclusive result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic...
The Issue: Potential for an electrical component of the O-arm" O2 Imaging System to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC-Intended for tightening...
The Issue: Stardrive Screwdrivers manufactured without a 5-degree relief cut around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EsoFLIP Recalled by Covidien, LLC Due to Due to saline conductivity issues,...
The Issue: Due to saline conductivity issues, their is a potential that dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasySuite 4K Integrated Operating Room System Model/Catalog Number:...
The Issue: A subset of the ES4K systems do not have complete records for earth leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate2 8F x 85cm Recalled by Stryker Neurovascular Due to Neurovascular...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Pro 14 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Anti-TG Ab Catalog # L2KTG6 (600 Tests) Recalled by Siemens...
The Issue: The potential for falsely elevated patient sample results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo ProVue Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro .014"guide wire Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAC 044 115cm Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...
The Issue: There is the potential that an electroneurodiagnostic medical device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo NXT ProVue 3 x 32 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.