Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,619 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,619 in last 12 months

Showing 3398134000 of 55,896 recalls

Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estradiol Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Testosterone Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Levonorgestrel Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estrone Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co. Due to...

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Ethinyl Estradiol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estradiol Micronized Bulk Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estriol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co. Due to...

The Issue: cGMP Deviations; lack of quality assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 23, 2017· Merit Medical Systems, Inc.

Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...

The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Sysmex America Inc

Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...

The Issue: Reported customer complaints of automated hematology analyzers catching fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Toshiba American Medical Systems

Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...

The Issue: It was discovered during a procedure that when the operator made an exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX Recalled by Zimmer...

The Issue: pegs shearing post-operatively

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Cook Medical Incorporated

Recalled Item: Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic...

The Issue: There have been five reports of graft thrombosis/occlusion during global...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper Release 8.2 (Laird chiller is always installed) Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: UNIQ: UNIQ FD10 722026 Recalled by Philips Electronics North America...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: The following systems are only affected if a Laird chiller Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· ReFlow Medical

Recalled Item: Wingman 35 Crossing Catheter Recalled by Medical Due to Medical is recalling...

The Issue: Medical is recalling the Wingman 35 Crossing Catheter because it may be...

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

Class I — Serious Health HazardOngoing
DrugMarch 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Pilocarpine Hydrochloride Ophthalmic Solution 4% Recalled by Novartis...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund