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. 1,098 recalls have been distributed to New York in the last 12 months.
Showing 17821–17840 of 55,896 recalls
Recalled Item: Gang Cath Lab Set Recalled by Smiths Medical ASD Inc. Due to Specific lots...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...
The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...
The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnia Soft Tissue Punch is a dental instrument designed to Recalled by Omnia...
The Issue: Omnia SRL received a notification from the contract manufacturer informing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PremierZen Platinum 5000 Recalled by Na Na Collection Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Krazy Night capsule Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triple SupremeZen Gold 3500 Recalled by Na Na Collection Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shogun-X capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs up 7 Red 70K capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Motha Jelly Crystals - Mango Flavoured Jelly Recalled by USA LANKA INC Due...
The Issue: Jelly contains undeclared FD&C Yellow #5 and FD&C Yellow #6
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Motha Jelly Crystals Strawberry Flavoured Jelly Recalled by USA LANKA INC...
The Issue: Jelly contains undeclared FD&C Red #40
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Motha Jelly Crystals - Black Currant Flavoured Jelly Recalled by USA LANKA...
The Issue: Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Motha Jelly Crystals - Orange Flavoured Jelly Recalled by USA LANKA INC Due...
The Issue: Jelly contains undeclared FD&C Yellow #6
Recommended Action: Do not consume. Return to store for a refund or discard.