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 19621–19640 of 28,355 recalls
Recalled Item: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...
The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNRISE instrument. The INFINITE F50 instrument is a 96-well absorbance...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Infinite M1000 PRO The Tecan Infinite M1000 PRO is Recalled by Tecan...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Infinite M1000 The Tecan Infinite M1000 is a multifunctional Recalled...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Infinite 200. The SUNRISE instrument is a 96-well absorbance Recalled...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 PRO The Tecan Infinite 200 PRO is a Recalled by Tecan US, Inc....
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Recalled by GE OEC Medical Systems, Inc Due to A firmware issue in...
The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to A firmware...
The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large QWIX Compression screw Recalled by Integra LifeSciences Corp. Due to...
The Issue: Labeling on the Qwix Screw product states that it is a "compression screw"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen Recalled by...
The Issue: Device can fail during operation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS Sterile Transparent Film and all the RENASYS Dressing kits Recalled...
The Issue: Sterility seal integrity failures on the Renasys Sterile Transparent Film
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Recalled by...
The Issue: Incorrect drill protocol in the Instructions for Use (IFU)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE IMPERVIOUS GOWN WITH THUMBHOOKS Recalled by Cardinal Health Due to Blue...
The Issue: Blue Impervious Gown with thumbhooks, X-large. All lots do not meet design...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology CT Model number 728244 Product Usage: Computed...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.