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. 2,628 recalls have been distributed to Arkansas in the last 12 months.
Showing 6541–6560 of 28,355 recalls
Recalled Item: Patient Information Center iX Recalled by Philips North America Due to...
The Issue: During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Distal Cover Model Number MAJ-2315 used with Recalled by...
The Issue: The Single Use Distal Cover MAJ-2315 may cause mucosal injury and/or become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs (1) 89-10529.04 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products HbA1c Reagent Kit- IVD for the quantitative...
The Issue: Potential for both unexpected positive and negative HbA1c results, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P)180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Set2Go Ventilation 12 (A) Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seattle PAP Plus Recalled by Draeger Medical, Inc. Due to Glued connections...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT (P)180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Set Coax 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist catheter is an intravascular micro axial...
The Issue: The Impella 5.5 pump experienced a heightened complaint rate for purge leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventstar Coax Recalled by Draeger Medical, Inc. Due to Glued connections of...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P)250 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kit Coax 3 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventstar Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kit Coax 1 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.