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. 2,491 recalls have been distributed to Arkansas in the last 12 months.
Showing 18881–18900 of 28,355 recalls
Recalled Item: ReliOn FastA1C Test Recalled by Polymer Technology Systems Due to A...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Systems (professional use product) Recalled by Polymer Technology...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health At Home A1C Test Kit Recalled by Polymer Technology Systems Due...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...
The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...
The Issue: The interface between the TB3 back and tilt base can separate when tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A...
The Issue: A complaint of the PRO2 jaw breaking prior to surgery being performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Ocean Blood Recovery Drains as follows: 2050-000 Ocean...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentraLink¿ Data Management System Software Versions: v13x Recalled by...
The Issue: There is a remote possibility CentraLink may download an order to the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.