The Recall Desk

Hazard

Documentation Failure recalls

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

What the numbers show

Total
6
Critical
0
Severe
0
Most recent
2024-08-28

Of the 6 documentation failure 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 documentation failure 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.

1–6 of 6

  • HighFDA (Devices)·Z-2581-2024·2024-08-28

    Baxter Spectrum Wireless Battery Modules May Fail to Document Infusion Status

    Baxter Spectrum Wireless Battery Modules may fail to automatically transmit infusion status information to hospital electronic medical records systems. The software issue affects 17,377 units nationwide.

    Product
    Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following: 35700BAX2 (Spectrum V8 infusion pump) or 3570009 (Spectrum IQ infusion pump) Baxter SIGMA Spectrum V8 Infusion Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2582-2024·2024-08-28

    Spectrum Wireless Battery Modules fail to auto-document infusion status

    Spectrum Wireless Battery Modules may fail to send infusion status updates to hospital electronic medical records. The issue affects 17,377 units nationwide used with Spectrum V8 and IQ infusion pumps.

    Product
    Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (Spectrum IQ infusion pump)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2438-2024·2024-07-31

    Sensis Vibe diagnostic systems software crash during event documentation

    Siemens Sensis Vibe diagnostic systems may crash when using documentation features during once-per-study event reporting. Three systems are affected; no injuries reported.

    Product
    Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as wel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0009-2021·2020-10-14

    Nettle Meadow Fig Honey Fromage Frais Recalled for Pasteurization Record Failure

    LuMaZu, LLC dba Nettle Meadow is recalling Fig Honey Fromage Frais because pasteurization temperatures were not recorded for two lots due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese *** Fig Honey Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz.***"
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0010-2021·2020-10-14

    Nettle Meadow Apple Cider Fromage Frais Recalled Due to Pasteurization Record Failure

    LuMaZu, LLC dba Nettle Meadow is recalling 5 oz. Apple Cider Fromage Frais because pasteurization temperatures were not recorded for two lots due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese ***Apple Cider Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz."
    Category
    Food
    Distribution
    8 states
  • LowFDA (Food)·F-1135-2018·2018-05-02

    Italian Rose Garlic Spread Recalled for Documentation and Monitoring Failures

    Italian Rose Garlic Products, LLC is recalling 842 pails of Italian Rose Garlic Spread because the firm failed to document mixing times and monitor pH levels during production.

    Product
    ITALIAN ROSE GARLIC SPREAD, Gluten Free, NET WT. 35 LB (16 kg), www.italian-rose.com, Riviera Beach, FL 33404
    Category
    Food
    Distribution
    1 state