The Recall Desk

Hazard

Allergy recalls

3 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
3
Critical
0
Severe
1
Most recent
2016-01-08

Of the 3 allergy recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (33%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all allergy recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–3 of 3

  • HighUSDA FSIS·005-2016·2016-01-08

    New York Style Sausage Co. Recalls Pork Sausage Due to Undeclared Sheep Casings

    New York Style Sausage Co. is recalling approximately 4,040 pounds of pork sausage because the products use sheep casings that are not declared on the label, posing an allergy risk.

    Product
    NEW YORK STYLE SAUSAGE CO. — New York Style Sausage Co. Recalls Pork Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0499-2016·2015-12-09

    Life Science Pharmacy Recalls BI-EST Suspensions Due to Penicillin Contamination

    Life Science Pharmacy Inc. is recalling BI-EST Suspensions because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.

    Product
    BI-EST Suspensions, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2002-2014·2014-07-16

    3M Attest Auto-reader Recalled for Missing Dry Natural Rubber Labeling

    3M is recalling Attest Auto-readers because labels failed to disclose dry natural rubber content, posing an allergy risk.

    Product
    3M Attest Auto-reader. Model numbers 390, 390G,and 490. These devices incubate the biological indicators (BIs) to determine a positive or negative result for the sterilization cycle.
    Category
    Medical Device
    Distribution
    Distributed nationwide