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. 2,574 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,574 in last 12 months

Showing 4186141880 of 55,896 recalls

Medical DeviceJuly 15, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ CREA (Creatinine) and Dimension Vista¿ CREA (Creatinine) Recalled...

The Issue: Siemens has confirmed that the Dimension CREA and Dimension Vista CREA may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2015· Iris Diagnostics

Recalled Item: iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049 Recalled by...

The Issue: Iris International is recalling the iChemVELOCITY systems because they do...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2015· Medtronic Cardiovascular Surgery-the Heart Valve Division

Recalled Item: EnVeo R Loading System Recalled by Medtronic Cardiovascular Surgery-the...

The Issue: Medtronic is recalling the EnVeo R Loading Systems because of the presence...

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

Class I — Serious Health HazardOngoing
DrugJuly 14, 2015· KVK-Tech, Inc.

Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK-Tech, Inc. Due to Failed...

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

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 14, 2015· Ortho Solutions Inc

Recalled Item: Ortho OS Solutions UltOS 3.5mm locking screw 12mm to 50mm Ortho Solutions...

The Issue: Ortho Solutions Inc is initiating a recall on behalf of UltOS 3.5mm locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: cobas b 123 Fluid Pack COOX 400 Product Recalled by Roche Diagnostics...

The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: cobas b 123 Fluid Pack COOX 200 Product Recalled by Roche Diagnostics...

The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...

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

Class II — Potential Health HazardOngoing
DrugJuly 13, 2015· Life and More LLC

Recalled Item: Akttive High Performance Fat Burner Gold dietary supplement capsules...

The Issue: Marketed Without An Approved NDA/ANDA: Dietary supplements contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 13, 2015· Perrigo Israel Pharmaceuticals

Recalled Item: Mometasone Furoate Ointment USP Recalled by Perrigo Israel Pharmaceuticals...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugJuly 13, 2015· Purdue Pharma L.P.

Recalled Item: Intermezzo (zolpidem tartrate) Recalled by Purdue Pharma L.P. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 13, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....

The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....

The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Sedecal S.A.

Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....

The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2015· Draeger Medical, Inc.

Recalled Item: PS500 of an IACS Workstation Critical Care (Evita Infinity V500) Recalled by...

The Issue: The battery capacity of the optional PS500 of an IACS Workstation Critical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2015· Etac Supply Center Ab

Recalled Item: Etac Relax wall mounted shower seat The Etac Relax is Recalled by Etac...

The Issue: The recalling firm has received reports of a malfunction of the Relax wall...

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

Class II — Potential Health HazardOngoing
FoodJuly 10, 2015· Maya Overseas Foods,Inc

Recalled Item: A Taste of the East maya brand Cashew Split Recalled by Maya Overseas...

The Issue: The cashews have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 10, 2015· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery Recalled by...

The Issue: Stryker Sustainability Solutions has received reports indicating that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...

The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2015· Hardy Diagnostics

Recalled Item: HardyCHROM MRSA Cat no: G307 Lot no: H15155 Expires: 2015-08-13 Recalled by...

The Issue: Hardy Diagnostics is recalling HardyCHROm MRSA due to a report of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2015· Cadence Inc.

Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...

The Issue: Graduation marks of the syringe are not centered with the numeric position...

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

Class II — Potential Health HazardOngoing