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. 2,451 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,451 in last 12 months

Showing 2578125800 of 28,355 recalls

Medical DeviceJune 21, 2013· MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK

Recalled Item: MHI-TM2000 Linear Accelerator System Recalled by MITSUBISHI HEAVY...

The Issue: Software anomaly: Mitsubishi Heavy Industries, Ltd. became aware of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 10mL Product Number: 10-1000 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-1.0 mL LeGoo with 3 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 5mL Product Number: 10-0500 LeGoo is Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 0.5 mL LeGoo with 3 Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Endovascular Occlusion Gel 0.5 mL Product Number: LG50IT LeGoo...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo w/ no Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder .25mL Product Number: 10-0025 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Endovascular Occlusion Gel 1.0 mL Product Number: LG100IT LeGoo...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Endovascular Occlusion Gel 2.5 mL Product Number: LG250IT LeGoo...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 1mL Product Number: 10-0100 LeGoo is Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo with 3 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder .5mL Product Number: 10-0050 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo with 3 Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo w/ no Cannula Product...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.25 mL LeGoo with 3 Cannula Pouch...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2013· Haemonetics Corporation

Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...

The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Carestream Health Inc.

Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...

The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...

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

Class II — Potential Health HazardOngoing