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. 2,661 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,661 in last 12 months

Showing 27212740 of 28,355 recalls

Medical DeviceOctober 16, 2024· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Positioner. Model Number C-XP-5000Z Recalled by Maquet...

The Issue: Deviations in the manufacturing process created a compromise in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter AK 98 Dialysis Machine Recalled by Baxter Healthcare Corporation Due...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Pacer Implant Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Some of the suture packages within the convenience kits contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Open Heart CDS Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Some of the suture packages within the convenience kits contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Shoulder Repair Pack-LF Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Some of the suture packages within the convenience kits contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· Draeger Medical, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...

The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2024· Draeger Medical, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...

The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2024· Karl Storz Endoscopy

Recalled Item: 4.5 x 180 mm Aggressive Cutter Recalled by Karl Storz Endoscopy Due to Due...

The Issue: Due to holes detected in the inner barrier system that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively...

The Issue: May Generate Negatively Biased Results When Testing Samples with High...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2024· Hologic, Inc

Recalled Item: BioZorb Marker. Radiographic soft tissue marker. Recalled by Hologic, Inc...

The Issue: Firm received reports of adverse events/complications that include serious...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2024· Philips Medical Systems Technologies Ltd.

Recalled Item: Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to Recalled by...

The Issue: A software issue affecting Philips Vue PACS may cause incorrect ischemic map...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: PORT INSERTION PACK Recalled by MEDLINE...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE medical convenience kits labeled as: 1) ACETABULAR PACK-LF Recalled...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) ANGIO PACK #2 Recalled by MEDLINE...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: L&D MINOR PACK Recalled by MEDLINE...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) C-SECTION OR 30 CDS Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: COLON WOUND CLOSURE PACK Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) MAJOR VASCULAR-LF Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK Recalled by MEDLINE...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) BURN Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing