The Recall Desk

Hazard

Shelf Life Stability recalls

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

What the numbers show

Total
5
Critical
0
Severe
0
Most recent
2017-05-10

Of the 5 shelf life stability recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 shelf life stability 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.

1–5 of 5

  • ModerateFDA (Devices)·Z-1915-2017·2017-05-10

    Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Stability Data

    Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, THIN OSTEOTOME BLADE, 12 MM X 3 INCH, REF 71369212, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1919-2017·2017-05-10

    Smith & Nephew Recalls Osteotome Blades Due to Shelf Life Data

    Smith & Nephew is recalling 1,741 units of Renovation osteotome blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, ROUNDED END, THIN OSTEOTOME BLADE, 12 MM, REF 71369412, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1843-2015·2015-07-01

    Siemens IMMULITE 2000 Italian Cypress Allergy Test Recall

    Siemens is recalling specific lots of the IMMULITE 2000 Italian Cypress 3g Allergy test because they fail to meet shelf-life stability specifications.

    Product
    IMMULITE 2000/IMMULITE 2000 XPi Italian Cypress 3g Allergy, Catalog # T23L4 (40 test), Siemens Material Number (SMN) 10386079, IVD. For in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers for the quantitative measurement of allergen-specific IgE in human serum, as
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-1008-2013·2013-03-06

    Aptalis Recalls SourceCF Pediatric Multivitamin Drops Due to Shelf Life Concerns

    Aptalis Pharma is recalling SourceCF Pediatric Drops because the formulation may not support the labeled shelf life. The recall covers 14,439 units distributed in the US, Italy, Canada, and Brazil.

    Product
    SourceCF(R) Pediatric Drops, Multivitamins with A, B, D, E and K Plus Zinc, 2 FL OZ. (60ML), NDC 66212-300-60, UPC 668212300600
    Category
    Drug
    Distribution
    Distributed nationwide