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. 2,666 recalls have been distributed to Arkansas in the last 12 months.
Showing 181–200 of 28,355 recalls
Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...
The Issue: The mix up of the impression caps provided in the package. The provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION Recalled by Medline...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile Saline Wound Wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer STERILE saline wound wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n)...
The Issue: Potential risk of Quality Control failures and/or false resistant antibiotic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raz-AT (Attendant Tilt) Mobile Shower Commode Chair Recalled by Raz Design...
The Issue: Due to a modification by a vendor and may be reinstalled without properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. Recalled by AVID Medical,...
The Issue: Tyvek bag seal issue which may compromise sterility of the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number:...
The Issue: Products were mislabeled as the 6mm product but included the 5 mm product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET...
The Issue: Under circumstances involving exposure to particular chemicals and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEAR Implant. Model Number: 1000. Recalled by Miach Orthopaedics Due to...
The Issue: Incorrect expiration date on label that extends beyond the product's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 Surgeon Console Viewer Display Recalled by Intuitive Surgical,...
The Issue: Robotic-assisted surgical system has Viewer Display manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.