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. 2,638 recalls have been distributed to New York in the last 12 months.
Showing 32001–32020 of 55,896 recalls
Recalled Item: AVID TruCustom PLASTIC BASIN PACK convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom GYN LAPAROSCOPY convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAN OF STEEL capsules Recalled by Vitility Due to Undeclared Sildenafil
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUELICIN (Succinylcholine Chloride) Injection Recalled by Advanced Pharma...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specifications: out of specification observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 10 Recalled by SCA...
The Issue: Lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Inside Bender (L) and (R). Part of MAXIMIS Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Nut Inserter B. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 5.5 mm Instrument Tap. Part of MAXIMIS Pedicle Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 80mm Curved Rod. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 30mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 120mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 50mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Nut Driver 4.0 Hexa and Alignment Driver. Part Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.