New York recalls
4035 federal recalls on file affecting New York - 954 New York-specific plus 3081 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 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.
- 2012-10-10FDA-DeviceBeckman CoulterClass IINationwideCOULTER PrepPlus, Part Number: 286600 Product Usage: The COULTER PrepPlus, is a microprocessor-controlled pipetting and diluting system, designed for automating sample preparation or assay methods. It is capable of aspirating and dispensing liquid samples.
The recall was initiated because Beckman Coulter has confirmed that the Coulter PrepPlus may experience intermittant reagent level sense failures where the instrument may not produce a warning that a reagent vial is low or out of reagent.
- 2012-10-10FDA-DeviceSynthesClass IINationwideCheck Synthes MIRS spine system labeling
Synthes is initiating a Medical Device Labeling Correction following a detailed review of the current labeling in response to reported complaints. Synthes has identified technique measures and has updated the labeling associated with this system. The labeling reflects updated technique recommendations and emphasizes the importance of avoiding rod mis-alignment.
- 2012-10-10FDA-FoodBliss UnlimitedClass IINationwideStop using Luna & Larry's Coconut Bliss Mocha Maca Crunch
Recent tests show that one lot of the raw material, Casa de Mesquite brand Mesquite Bean flour, has the potential to be contaminated with Bacillus cereus, a spoilage organism which can cause diarrhea, nausea and other symptoms
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