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. 2,502 recalls have been distributed to Arkansas in the last 12 months.
Showing 18461–18480 of 28,355 recalls
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software...
The Issue: Software anomaly; Thermo-Fisher Scientific initially discovered and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specimen Gate Laboratory Recalled by PerkinElmer Life and Analytical...
The Issue: Potential for errors in patient results generated by the Specimen Gate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...
The Issue: Surgical technique was revised to prevent static plate screws blocking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software changes now available to address several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...
The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software changes now available to address several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip Recalled by...
The Issue: Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PreludeSYNC Radial Compression Device is a sterile Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Sodium Chloride Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...
The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.