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.

49,990 total recalls
2,491 in last 12 months

Showing 2048120500 of 28,355 recalls

Medical DeviceFebruary 29, 2016· Karl Storz Endovision, Inc.

Recalled Item: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use Recalled by...

The Issue: Endoscope cleaning brush 11276CL may not fit resulting in an inability to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...

The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...

The Issue: Dialyzer header leak due to possible improper torque

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...

The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Papoose Infant Spine Immobilizer Item # Item Description: PA-100 Papoose...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Undersleeve Gray Product Usage: Knee undersleeves are worn as Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Diabetic Walker Product Usage: Rebound Diabetic Walkers are used...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Air Walker Product Usage: Rebound Air Walkers are indicated Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Product Usage: Rebound Cartilage is an external knee...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Product Usage: Unloader Custom is an external knee Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Lite Product Usage: Unloader Custom Lite is an Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ab Sciex

Recalled Item: Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the Recalled by Ab...

The Issue: Wrong quantitative results may be displayed in a report from the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: NecLoc Extrication Collar Product Usage: Necloc collars are applied to...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Purewick Corporation

Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...

The Issue: PureWick is recalling external catheter for women Wicks because the labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Miami J Collar Product Usage: Miami J collars are applied Recalled by Ossur...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

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

Class II — Potential Health HazardOngoing