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. 2,189 recalls have been distributed to New York in the last 12 months.
Showing 5161–5180 of 55,896 recalls
Recalled Item: Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25...
The Issue: Elevated lead levels in cinnamon
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...
The Issue: During manufacturing, the last three tests from the 160 test flex of lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scortisoara macinata/ Ground cinnamon Recalled by MAMTAKIM, Inc. Due to...
The Issue: MAMTAKIM Inc.,888 Magnolia Ave, Elizabeth NJ 07201 is initiating a recall of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VEGAN OAT Recalled by Van Leeuwen Ice Cream LLC Due to Undeclared Peanuts
The Issue: Undeclared peanuts (allergen)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...
The Issue: Potential for the front lever chain of the DR 800 table to fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progesterone Injection Recalled by Eugia US LLC Due to Presence of...
The Issue: Presence of Particulate Matter: Complaint received of a glass particle in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Recalled by...
The Issue: Reports have been received regarding open seals on the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiomarC EX Fiducial Marker System Recalled by Carbon Medical Technologies,...
The Issue: This recall has been initiated due to a failure to provide an MRI Insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (250 Test - REF)-In vitro diagnostic Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 (250 Test)-In vitro diagnostic use in Recalled by...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (250 Test)- In vitro diagnostic use Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.