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. 2,673 recalls have been distributed to New York in the last 12 months.
Showing 22821–22840 of 55,896 recalls
Recalled Item: Pasteurized Process American Cheese Recalled by Great Lakes Cheese Co Inc...
The Issue: 5 lb. loaves of cheese may contain metal foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pasteurized Process American Cheese Recalled by Great Lakes Cheese Co Inc...
The Issue: 5 lb. loaves of cheese may contain metal foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pasteurized Process American Cheese Recalled by Great Lakes Cheese Co Inc...
The Issue: 5 lb. loaves of cheese may contain metal foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pasteurized Process American Cheese Recalled by Great Lakes Cheese Co Inc...
The Issue: 5 lb. loaves of cheese may contain metal foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pasteurized Process American Cheese Recalled by Great Lakes Cheese Co Inc...
The Issue: 5 lb. loaves of cheese may contain metal foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prima Della Delicatessen Pasteurized Process Sharp American Cheese Recalled...
The Issue: 5 lb. loaves of cheese may contain metal foreign material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Levetiracetam Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert - the incorrect package insert...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS Recalled by AMD Medicom...
The Issue: Due to an error on the packaging line, some level 2 masks may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Through a customer complaint and and internal investigation it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 3 MASKS Recalled by AMD Medicom...
The Issue: Due to an error on the packaging line, some level 2 masks may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The firm has become aware that there is a likelihood that a missing snap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIARTICULAR PLATES - FEMUR Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Knee Systems Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prox Lat Tib Lock Plate and Dist Med Tib Lock Recalled by Zimmer Biomet,...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB PERIPROSTHETIC Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various temporary devices used during the implantation of the device...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.