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. 2,076 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,076 in last 12 months

Showing 62616280 of 28,355 recalls

Medical DeviceMay 18, 2023· Baxter Healthcare Corporation

Recalled Item: Allen Advance Chest Support with Pad Recalled by Baxter Healthcare...

The Issue: Potential for the device to crack where the Chest Base Prone support...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Bryan Medical Inc

Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling

The Issue: Devices were mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...

The Issue: A firmware error may lead to an incorrect association of test result(s) to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...

The Issue: Medtronic has identified that the logfiles downloaded from the recently...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...

The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· NeuMoDx Molecular Inc

Recalled Item: NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of...

The Issue: Potential for lot number discrepancies between the test strip packaging and...

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

Class III — Low RiskOngoing
Medical DeviceMay 15, 2023· Olympus Corporation of the Americas

Recalled Item: Always-On Tip Tracked Instruments (SPiN Drive instruments) Triple Needle...

The Issue: Electromagnetic (EM) sensor tracking malfunction impacts the use of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing