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. 2,491 recalls have been distributed to Arkansas in the last 12 months.
Showing 18861–18880 of 28,355 recalls
Recalled Item: Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N...
The Issue: Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...
The Issue: Reunion TSA Peg Alignment Sound broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...
The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...
The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...
The Issue: Edits to Particle field definition parameters may not be saved when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow SELF CHECK (European) Recalled by Polymer Technology Systems Due to A...
The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.