The Recall Desk

Hazard

Shipping Error 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
0
Most recent
2019-05-22

Of the 3 shipping error 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.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all shipping error 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

  • LowFDA (Devices)·Z-1363-2019·2019-05-22

    Abbott Technopath Multichem S Plus Level 2 Recalled for Missing Dry Ice

    Abbott Laboratories is recalling Technopath Multichem S Plus Level 2 quality control serum delivered to Latvia without required dry ice.

    Product
    Technopath Multichem S Plus Level 2 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1362-2019·2019-05-22

    Abbott Multichem S Plus Quality Control Serum Recalled for Missing Dry Ice

    Abbott Laboratories is recalling Technopath Multichem S Plus Level 1 quality control serum because units were delivered without required dry ice.

    Product
    Technopath Multichem S Plus Level 1 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0339-2014·2013-11-27

    Synovis Recalls Dura-Guard and Vascu-Guard Patches Due to Shipping Errors

    Synovis is recalling Dura-Guard and Vascu-Guard patches because specific units were shipped in divided cell configurations with a specific revision of the Instructions for Use.

    Product
    Dura Guard, Dural Repair Patch with Apex Processing. For use as a dura substitute for the closure of dura mater during neurosurgery. Product Code: DG0209SN DG0209SN DG0209SN DG0209SN DG0209SN DG0209SN DG0209SN DG0209SN DG0404SN DG040
    Category
    Medical Device
    Distribution
    Distributed nationwide