The Recall Desk

Hazard

Mis Packaging 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
2026-07-15

Of the 5 mis packaging 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 mis packaging 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

  • HighFDA (Food)·H-1150-2026·2026-07-15

    High Valley Orchard Chocolate Covered Raisins Recalled for Undeclared Peanut

    High Valley Orchard Chocolate Covered Raisins (15oz bags) are recalled nationwide due to undeclared peanut from mis-packaging. Consumers with peanut allergies should not consume this product.

    Product
    High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is packaged in clear plastic container. UPC on retail container: 0 952348 80170 0. The label of affected product declares: INGREDIENTS: MILK CHOCOLATE (SUGAR,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1612-2023·2023-05-24

    Reprocessed DVT Compression Sleeves Recalled Due to Labeling and Packaging Errors

    Stryker Sustainability Solutions recalls reprocessed DVT compression sleeves that may be mislabeled or mispackaged. These prescription-only devices could be improperly identified or distributed due to packaging errors.

    Product
    REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0836-2020·2020-01-29

    Paltop Dental Implant Recall Due to Incorrect Cover Screw Packaging

    Paltop Advanced Dental Solutions is recalling 67 dental implants because some were packaged with the wrong cover screw, preventing proper fit.

    Product
    Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2658-2017·2017-07-12

    Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-packaging Error

    Encore Medical is recalling 9 units of 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.

    Product
    3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2659-2017·2017-07-12

    Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging

    Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.

    Product
    3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to c
    Category
    Medical Device
    Distribution
    Distributed nationwide