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. 2,553 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,553 in last 12 months

Showing 1606116080 of 28,355 recalls

Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: KIT-DE-0080 BYPASS KIT LOHNE X1( Item KIT-DE-0080) Product Usage: The...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)KIT4184 APEN LOBECTOMY KIT X0 Item Number: KIT4184 APEN LOBECTOMY...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX LAPZD ZESTAW DO SG (2) BOX LAPISG1 ZESTAW Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2018· ConvaTec, Inc

Recalled Item: Convatec Esteem(TM) Synergy Stomahesive(R) Recalled by ConvaTec, Inc Due to...

The Issue: It was discovered that the stoma hole of one lots of the Esteem synergy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...

The Issue: The product packaging seal has the potential to experience seal creep. This...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...

The Issue: There is a potential for a software issue that may cause the need for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· LivaNova USA

Recalled Item: Sorin Stockert Heater-Cooler System 3T Recalled by LivaNova USA Due to Firm...

The Issue: Firm is notifying customers that the Deep-Cleaning Service is now available...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...

The Issue: There is a potential for a software issue that may cause the need for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· CareFusion 303, Inc.

Recalled Item: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...

The Issue: Complaints where users were unable to prime the administration set.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...

The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing