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. 1,173 recalls have been distributed to New York in the last 12 months.
Showing 6821–6840 of 55,896 recalls
Recalled Item: Sterile Diluent Recalled by Eli Lilly & Company Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tranquility & Teachings William Monague plate set Recalled by Canadian Art...
The Issue: Product has been recalled because it may exceed FDA guidance levels for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hood Country Style Cottage Cheese 24oz () Recalled by HP Hood (VERNON) Due...
The Issue: Undeclared pineapple, sugar, modified corn starch, natural flavors,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...
The Issue: System error messages may delay the ability to test patient samples and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...
The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...
The Issue: Due to a misaligned calibration of the wired controller that may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical 070 Reperfusion System Recalled by ROUTE 92 MEDICAL INC Due...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Full Length 070 Access System Recalled by ROUTE 92 MEDICAL...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device:...
The Issue: Degraded and unusable upon removal from the foil pouch due to exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INNOMED CUP REMOVAL STARTER INSTRUMENT Recalled by Innomed, Inc. Due to 54...
The Issue: 54 MM finisher blade was inadvertently affixed to the shaft of the CupX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Value Honey Roasted Cashews Recalled by John B. Sanfilippo & Son Inc....
The Issue: undeclared milk and coconut
Recommended Action: Do not consume. Return to store for a refund or discard.