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 20461–20480 of 28,355 recalls
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Gauze Sponges Recalled by Covidien LLC Due to Compromised sterility...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition: Intended to produce cross-sectional images of...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is Recalled by GE...
The Issue: Ferrous material in the SIGNA Pioneer Table Control Box (TCB) could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERION Unit (Vision Planner) Product Usage: The VERION Image Recalled by...
The Issue: Alcon is conducting a voluntary medical device correction of all VERION...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...
The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica ISE Module Calibrant A Recalled by AMS Diagnostics, LLC Due to Lot...
The Issue: Lot was not functioning properly and not exhibiting the correct physical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT-5100 (Epic 5100) and RT 3100 : Product Usage: Recalled by Nidek Inc Due...
The Issue: There has been a reoccurrence of an issue on the RT 5100 and RT 3100 of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...
The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.