New York recalls
4653 federal recalls on file affecting New York - 1028 New York-specific plus 3625 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2014-10-08USDAClass INationwideFirma De Minnesota Retira Del Mercado Productos De Carne De Res Y Aves Debido A Posible Contaminacion Con Listeria
Product Contamination
- 2014-09-06USDAClass IICheck Cookin' Good chicken packages
Processing Defect
- 2014-08-21USDAClass INationwideDo not eat APPA Fine Foods chicken caesar salad
Product Contamination
- 2014-08-12USDAClass IINationwideDon't eat Applegate Naturals chicken nuggets
Product Contamination
- 2014-08-09USDAClass IIINationwideCheck Oberto's chicken strips for swollen packages
Processing Defect
- 2014-08-06USDAClass INationwideDo not eat Cavanaugh Smoked Sausage
Misbranding, Unreported Allergens
- 2014-07-22USDAClass IINationwideDo not serve Sara Lee smoked sausage
Misbranding, Unreported Allergens
- 2014-06-27USDAClass IIStop eating Wegmans Organic Ham
Product Contamination
- 2014-06-19USDAClass INationwideDo not eat Thai Kitchen Chicken Pad Thai
Misbranding, Unreported Allergens
- 2014-06-11USDAClass IIDon't eat Fuitland American Meat beef products
Product Contamination
- 2014-05-21USDAClass INationwideDo not eat recalled Wegmans or Sugar Lake Farms chicken strips
Misbranding, Unreported Allergens
- 2014-04-24USDAClass IDo not eat Cobblestone Farms pork ribs
Produced Without Benefit of Inspection
- 2014-04-20USDAClass INationwideStop using Oscar Mayer Classic Wieners
Misbranding, Unreported Allergens
- 2014-04-19USDAClass INationwideDon't serve Sugar Lake Farms chicken breast products
Misbranding, Unreported Allergens
- 2014-04-02USDAClass INationwideDon't eat Backpackers Pantry fettuccini alfredo
Misbranding, Unreported Allergens
- 2014-04-01USDAClass IDon't eat AdvancePierre chicken breast fritters
Misbranding, Unreported Allergens
- 2014-03-26USDAPublic Health AlertNationwideDo not eat Nutriom egg products
Unfit for Human Consumption
- 2014-02-26USDAClass IDon't eat Flower or Fortune brand liver pâté
Produced Without Benefit of Inspection
- 2014-02-18USDAClass INationwideDo not eat Rancho Feeding Corporation beef
Produced Without Benefit of Inspection
- 2014-02-15USDAClass INationwideCheck OvaEasy egg products for Salmonella risk
Product Contamination
- 2014-02-11USDAClass IINationwideStop eating recalled beef jerky products from Utah
Misbranding, Unreported Allergens
- 2014-02-04USDAClass INationwideStop eating Healthy Choice chicken soup bowls
Misbranding, Unreported Allergens
- 2014-02-01USDAClass IINationwideCheck House of Smoke sausage and meat products
Misbranding, Unreported Allergens
- 2014-01-27USDAClass IINationwideUna Firma En Arkansas Retira Del Mercado Productos De Pollo Congelado Debido A Alérgenos No Identificados
Misbranding, Unreported Allergens
- 2014-01-19USDAClass IINationwideCheck your Velveeta mac and cheese for soy allergen
Misbranding, Unreported Allergens
- 2014-01-10USDAClass INationwideCheck institutional chicken products for recall
Product Contamination
- 2013-10-09FDA-DeviceCordisClass IINationwideCheck Cordis ADROIT 6F catheter lot numbers
Due to a labeling error related to the conversion of the inner diameter of the catheter from inches to millimeters. The English dimension is correct and is the primary dimension.
- 2013-10-09FDA-DeviceKing SystemsClass IINationwideCheck King LTS-D airway size labeling
On December 13, 2012, King Systems initiated a voluntary recall of one (1) case(s) (5) individual products) from one (1) lot [(IV1V3) 62 cases, 310 products]of King LTSD Oropharyngeal Airways because the package label indicated that the airway was a size 5 when in fact the airway in the package was a size 4. When King manufacturers a lot, all of the components are the same size, part number etc. I
- 2013-10-09FDA-DeviceMaquetClass IINationwideContact Maquet about Ultima OPCAB blade mislabeling
MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers OM-2003S & OM-2001D). Labeling for the 2 blade lots had been incorrectly applied. The standard blades from Lot #25052176 were incorrectly labeled as deep blades, and the 20 deep blades from Lot #25052200 were incorrectly labeled as standard blades.
- 2012-10-10FDA-DeviceBeckman CoulterClass IINationwideStop using Beckman Coulter RF reagent lots M012376, M101865
The recall was initiated because Beckman Coulter has confirmed customer reports of QC shifts, lot-to-lot variation, and an increase in the percent of patient samples recovering >20 IU/mL using the Lots# M012376 and M101865 of IMMAGE RF reagent. The lots identified for the RF reagent might produce false abnormal results.
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