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 21–40 of 28,355 recalls
Recalled Item: Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE Recalled by Medline...
The Issue: Fabric may experience premature delamination when using included laundering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN Recalled by Medline...
The Issue: Fabric may experience premature delamination when using included laundering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP. Product Code: 0046-0011. Recalled by Abiomed, Inc. Due to...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITY II Laser System Recalled by Lutronic Corporation Due to Reports of...
The Issue: Reports of devices sparking/popping and potentially burning patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029....
The Issue: During the bulk packaging process, some Luer Slip syringes were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP with SmartAssist. Product Code: 0046-0035. Recalled by Abiomed,...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist. Product Code: 1000323. Recalled by...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B12 System Model Numbers:(1) 722067 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M12 System Model Numbers: (1)722227 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M12 System Model Numbers: (1)722078 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 System Model Numbers: (1)722079 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M15 System Model Numbers: (1) 722064 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 System Model Numbers: (1) 722063 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M20 System Model Numbers: (1)722228 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B20 System Model Numbers: (1)722068 Recalled by PHILIPS MEDICAL...
The Issue: Under certain conditions, the table may move unexpectedly when the Reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 IABP. Software Version CS300 IABP C.01. Recalled by Datascope Corp....
The Issue: The firm has identified that the battery runtime and cycle specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 IABP. Software Version CS100 IABP Q.01. Recalled by Datascope Corp....
The Issue: The firm has identified that the battery runtime and cycle specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adapt Pump Recalled by Agiliti Health - Ellis Due to Agiliti identified an...
The Issue: Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONARCH Platform Recalled by Auris Health, Inc Due to Device for...
The Issue: Device for bronchoscopic visualization, patient airway access has software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm...
The Issue: Due to a need to update the product labeling (Instructions for Use IFU) as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.