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. 2,548 recalls have been distributed to Arkansas in the last 12 months.
Showing 16961–16980 of 28,355 recalls
Recalled Item: BO-TOP 20705 SMALL PATIENT 1/4 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICU ECC Pack BEQ-TOP 39202 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 49101 Childrens Large ECC Pack Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-T 25502 1/4 Better Bladder Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 38900 ECC PACK Recalled by Datascope Corporation Due to The Better...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory Recalled by Datascope Corporation Due to...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECC Small - Respiratory BEQ-TOP 5210 Recalled by Datascope Corporation Due...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-TOP 13901 RAPID RESPONSE Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ECC Pack BEQ-TOP 22300 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 33700 ECC 3/8" PACK Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22301 Recalled by Datascope Corporation Due to The Better Bladder...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 27610 ECC PACK 3/8 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22300 Recalled by Datascope Corporation Due to The Better Bladder...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22702 ECC W/HMOD 30000 Recalled by Datascope Corporation Due to The...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22701 Recalled by Datascope Corporation Due to The Better Bladder...
The Issue: The Better Bladder device provided as part of some custom tubing kits has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...
The Issue: Teleflex is recalling these products because the jaws of the tool tip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.