The Recall Desk

Hazard

Missing Label recalls

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

What the numbers show

Total
41
Critical
2
Severe
2
Most recent
2026-05-06

Of the 41 missing label recalls we have scored against our rubric, 2 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (5%) 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 missing label 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.

26–41 of 41

  • HighNHTSA·22V283000·2022-04-27

    School buses missing warning label for inoperative collision mitigation system

    Navistar is recalling certain 2022-2023 IC BUS school buses because the warning label for the inoperative collision mitigation system may be missing. Drivers may not be aware the safety system is not functioning.

    Product
    IC BUS — IC BUS RESB, CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V086000·2022-02-16

    2019 Volkswagen Atlas: Missing GVWR Label on Side-Step Models

    Volkswagen is recalling certain 2018-2021 Atlas and Atlas Cross Sport vehicles equipped with side steps due to a missing GVWR label that reflects the additional weight, increasing overloading risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0462-2022·2022-01-26

    Semglee Insulin Glargine Prefilled Pens Missing Label

    Mylan Pharmaceuticals is recalling approximately 73,175 Semglee (insulin glargine) prefilled pens nationwide because some units have a missing label. Patients should check their pens and contact their pharmacist or doctor if affected.

    Product
    Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled Pens per carton (NDC 49502-0196-75), Rx only, Manufactured in Malaysia for: Mylan Specialty L.P., Morgantown, WV, 26505.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0368-2022·2022-01-19

    Oxycodone Hydrochloride Oral Solution recalled for missing label

    Akorn, Inc. is recalling Oxycodone Hydrochloride Oral Solution 5 mg per 5 mL distributed nationwide due to missing label.

    Product
    Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 --- NDC 50383-961-34
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0367-2022·2022-01-19

    Morphine Sulfate Oral Solution 20 mg/mL recalled for missing label

    Akorn, Inc. is recalling Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) in 30 mL bottles nationwide due to missing labeling on approximately 10,836 bottles.

    Product
    Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles, Rx only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 -- NDC 50383-965-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2338-2021·2021-09-01

    MRI System Table Pads Missing Required Natural Rubber Allergen Label

    Table pads in Hitachi's ECHELON Oval MRI System contain natural rubber but lack required labeling on packaging and in user manuals. Federal regulations under 21 CFR 801.437 mandate disclosure of this material.

    Product
    ECHELON Oval MRI System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2498-2019·2019-10-02

    Philips Recalls Two DigitalDiagnost C50 X-ray Systems for Missing Labels

    Philips Healthcare is recalling two DigitalDiagnost C50 stationary X-ray systems in Puerto Rico due to a missing label identified during recent evaluations.

    Product
    DigitalDiagnost C50, Stationary X-ray System
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0361-2019·2018-11-07

    Inpeco FlexLab and Accelerator a3600 Recalled for Missing Safety Labels

    Inpeco S.A. is recalling 679 laboratory automation systems because some modules are missing safety pacemaker labels. The recall addresses a risk of pacemaker malfunction for personnel working near the equipment.

    Product
    FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) (same product) FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre- Analytical and Post-Analytical processing,
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2177-2017·2017-06-07

    AbbVie Recalls PEG Kits Due to Missing or Duplicate Components

    AbbVie is recalling specific lots of PEG Kits due to potential defects including missing components, duplicate parts, or missing labels and instructions.

    Product
    AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0897-2017·2016-12-28

    PerkinElmer Recalls EnLite Neonatal TREC Kits for Missing UDI Labels

    PerkinElmer is recalling 73 EnLite Neonatal TREC Kits because the Unique Device Identifier (UDI) is missing from the outer box labels.

    Product
    EnLite Neonatal TREC Kit;an in vitro diagnostic device intended for the semi-quantitative determination of TREC (T-cell receptor excision circle) DNA in blood specimens dried on filter paper. The test is for use on the VICTOR" EnLite instrument. The test is indicated for use as
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·15V856000·2015-12-21

    Starcraft RV Recalls 2015-2016 Trailers for Missing Sewer Valve Label

    Starcraft RV is recalling 2015-2016 Autumn Ridge and Solstice fifth wheel trailers because a missing caution label may allow sewer gas to enter the vehicle.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT SOLSTICE, AUTUMN RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide