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. 1,914 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,914 in last 12 months

Showing 3166131680 of 55,896 recalls

Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Titanium Calibrated Reaming Rod Recalled by Synthes (USA) Products...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 3.0 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Guide Rod Recalled by Synthes (USA) Products LLC Due to Possible lack...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Molnlycke Health Care, Inc

Recalled Item: 9x15" Medium Utility Positioner with Cover Recalled by Molnlycke Health...

The Issue: Products may not meet specifications due to possible presence of metal shavings.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Molnlycke Health Care, Inc

Recalled Item: 7x10" Small Utility Positioner with Cover Recalled by Molnlycke Health Care,...

The Issue: Products may not meet specifications due to possible presence of metal shavings.

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

Class II — Potential Health HazardOngoing
DrugJuly 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

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

Class III — Low RiskOngoing
Refund
FoodJuly 25, 2017· Gold Medal Products Co

Recalled Item: CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 Recalled by Gold...

The Issue: Missing ingredient statement on the label and undeclared soy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 25, 2017· Arrow International Inc

Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...

The Issue: Finished good kits may contain incorrect components. Kits that should...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2017· Arrow International Inc

Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...

The Issue: Finished good kits may contain incorrect components. Kits that should...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2017· Siemens Medical Solutions USA, Inc.

Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...

The Issue: Siemens is releasing a letter to inform about potential data loss relevant...

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

Class II — Potential Health HazardOngoing
DrugJuly 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2017· Teva Pharmaceuticals USA

Recalled Item: Famotidine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specification; out of specification for tablet weight

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2017· Epimed International

Recalled Item: RX-2 COUDE Epidural Needle Recalled by Epimed International Due to Potential...

The Issue: Potential for partially incomplete seal of product, impacting sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Epimed International

Recalled Item: TUOHY Epidural Needle Recalled by Epimed International Due to Potential for...

The Issue: Potential for partially incomplete seal of product, impacting sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Epimed International

Recalled Item: COUDE Blunt Nerve Block Needle Recalled by Epimed International Due to...

The Issue: Potential for partially incomplete seal of product, impacting sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Sorin Group Italia SRL - CRF

Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...

The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Sorin Group Italia SRL - CRF

Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...

The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...

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

Class II — Potential Health HazardOngoing