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 6561–6580 of 28,355 recalls
Recalled Item: VentStar Basic (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 breathing bag Set (P) 110 Recalled by Draeger Medical, Inc. Due to...
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 HEPA Recalled by Draeger Medical, Inc. Due to...
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 230 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 Bag Set (N) 110 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 w/oLL Recalled by Draeger Medical, Inc. Due to...
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 (P) 150 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: ID Coax 180 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: RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml Recalled by...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...
The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT- whole-body computed tomography (CT) X-Ray System Model Number:...
The Issue: Potential for Incorrect Image Orientation resulting images may be flipped or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT- Whole-body computed tomography (CT) X-Ray System Model Number:...
The Issue: Potential for Incorrect Image Orientation resulting images may be flipped or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.