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. 2,619 recalls have been distributed to Arkansas in the last 12 months.
Showing 10241–10260 of 28,355 recalls
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-O303000 CONTROL Recalled by Medline Industries Inc Due to Medline...
The Issue: Medline Industries, Inc. is removing specific lots of STAT-Site¿ Controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35...
The Issue: Sterility may be compromised due to an unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris CO2MPACT Endoscopic Insufflator system Recalled by Northgate...
The Issue: An internal tubing component in the flow path was made with incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc....
The Issue: An internal tubing component in the flow path was made with incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...
The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm Recalled by Bard...
The Issue: Due to the Penetration Depth Switch used to select the desired penetration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2...
The Issue: Due to complaints received regarding missing lid magnets which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products VersaTips - Product Usage: used to dispense...
The Issue: A deformity affecting a specific lot of VITROS¿ Chemistry Products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Injectable CT Port insertion kits - Product Usage: is Recalled by...
The Issue: The 5F Dignity CT Port kits were packaged with the incorrect size port. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm Recalled by...
The Issue: incorrect device is contained in the package. The packaging label indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...
The Issue: The external drainage system failed to meet Pyrogen test requirements for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...
The Issue: The device catheter tip was cut off (no tip) and the product packaging was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.