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. 2,662 recalls have been distributed to Arkansas in the last 12 months.
Showing 1141–1160 of 28,355 recalls
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Radiology Solutions software version 14.2.2 Recalled by...
The Issue: Due to software issue, radiology reports may not be fully displayed when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT Recalled by...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. IQon Spectral CT Recalled by...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Big Bore RT Recalled by...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. CT 6000 Recalled by Philips...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance 16 Power Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT 728326 Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity Core128 Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT SP Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.