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. 1,834 recalls have been distributed to New York in the last 12 months.
Showing 41721–41740 of 55,896 recalls
Recalled Item: TRIMIX Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy Due to...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHYLCOBALAMIN MDV Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PYRIDOXINE HCL Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SERMORELIN/GHRP-6/GHRP-2 Recalled by JD & SN Inc., dba Moses Lake...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALPROSTADIL/PROCAINE Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...
The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/MR Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Philips Healthcare has become aware of a problem in which the Ingenuity TF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC) Recalled by...
The Issue: customers are receiving a high number of Abnormal Assay Errors or are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips GoSafe Mobile Help Button Recalled by Lifeline Systems, Incorporated...
The Issue: Irregular battery disconnection resulted in issues with Mobile Health Button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMES FARM GARDEN PEAS CHICHAROS Recalled by Restaurant Depot Due to...
The Issue: Jetro Restaurant Depot has initiated a recall due to Listeria monocytogenes...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Healthcare TraumaDiagnost Recalled by Philips Electronics North...
The Issue: If arm is not fastened securely it could fall down.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER ISOTON 4 Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...
The Issue: The end cap may loosen and detach making the instrument non-functional. No...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft...
The Issue: Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Pioneer Plus Re-Entry Catheter Recalled by Volcano Corporation Due...
The Issue: Due to a manufacturing defect, there is the possibility that a small wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that...
The Issue: The devices that included the OVAR research test were not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.