The Recall Desk

Hazard

Packaging Mismatch 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
2026-03-11

Of the 3 packaging mismatch 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 packaging mismatch 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

  • ModerateFDA (Devices)·Z-1493-2026·2026-03-11

    Advanced Bionics sound processor packaging label does not match contents

    Advanced Bionics is recalling two Sky CI M90 Sound Processors because the behind-the-ear sound processor packaging label differs from the product included in the pack.

    Product
    Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor Model/Catalog Number: CI-5295-150
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0773-2024·2024-01-31

    Stryker Tornier Shoulder Implant Recalled for Device Packaging Mismatch

    Tornier, Inc is recalling 50 units of Stryker Tornier Perform shoulder implants because the incorrect device is contained in the labeled package. Affected batch: lot 6714AZ, serial 001–050.

    Product
    Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0116-2021·2020-10-28

    Ethicon Recalls VICRYL Sutures Due to Packaging Mismatch

    Ethicon is recalling VICRYL sutures because the foil package may not match the label and carton. The incorrect suture differs in size, length, and construction.

    Product
    VICRYL MONOFILAMENT VIOLET 4IN (10CM) USP 10-0 (M0.2) SINGLE-ARMED CS140-6 - Product Usage: Intended for ophthalmic soft tissue approximation/ligation. Product Code: V960G
    Category
    Medical Device
    Distribution
    0 states