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. 1,837 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,837 in last 12 months

Showing 4048140500 of 55,896 recalls

Medical DeviceNovember 2, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...

The Issue: The firm has received 15 complaints over ten years related to the connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 2, 2015· Synthes (USA) Products LLC

Recalled Item: 2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended Recalled...

The Issue: It was discovered that the above part number and lot of 2.4mm Locking Screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2015· BioHorizons Implant Systems Inc

Recalled Item: RBT Recalled by BioHorizons Implant Systems Inc Due to An incorrect label...

The Issue: An incorrect label reading 10.5mm and not the specified 15mm was placed...

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

Class II — Potential Health HazardOngoing
DrugOctober 29, 2015· Amerisource Health Services

Recalled Item: HYDROCHLOROTHIAZIDE CAPSULES Recalled by Amerisource Health Services Due to...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 29, 2015· Green Organic Vegetables Incorporated

Recalled Item: Natures Promise Organic Edamame in Pod Recalled by Green Organic Vegetables...

The Issue: Product contains undeclared soy.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 29, 2015· Green Organic Vegetables Incorporated

Recalled Item: Natures Promise Organic Shelled Edamame Recalled by Green Organic...

The Issue: Product contains undeclared soy.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· NxStage Medical, Inc.

Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...

The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· NxStage Medical, Inc.

Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...

The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Defective Delivery System; potential to have inaccurate dosage delivery

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Defective Delivery System; potential to have inaccurate dosage delivery

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2015· Frozen Specialties Inc

Recalled Item: FOOD LION CHEESE microwaveable crispy thin crust pizza KEEP FROZEN Recalled...

The Issue: The product contains the Kosher symbol on its retail packaging. This symbol...

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

Class III — Low RiskOngoing
Refund
FoodOctober 28, 2015· Frozen Specialties Inc

Recalled Item: FOOD LION CHEESE crispy thin crust pizza KEEP FROZEN NET Recalled by Frozen...

The Issue: The product contains the Kosher symbol on its retail packaging. This symbol...

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

Class III — Low RiskOngoing
Refund