The Recall Desk

Hazard

Defective Valve 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
1
Most recent
2020-07-29

Of the 5 defective valve recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (20%) 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 defective valve 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 (Devices)·Z-2343-2018·2018-07-11

    B. Braun Recalls 26-Lead Transfer Sets for Valve Orientation Defect

    B. Braun Medical is recalling 26-Lead Transfer Sets for the APEX Compounding System because valves may be incorrectly oriented, posing a risk of unintended admixture.

    Product
    26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Devices)·Z-2234-2017·2017-06-14

    ConvaTec Recalls Non-Rebreather Masks Due to Potential Valve Defect

    ConvaTec, Inc. is voluntarily recalling specific lots of Non-Rebreather Masks due to a potential defect in the check valve. The recall covers units distributed in the US and internationally.

    Product
    Non-Rebreather Mask, Reservoir Bag, Check Valve, Two Side Valves, No Tubing, Product Code 226MM
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Drugs)·D-1341-2014·2014-05-28

    Teva Recalls QVAR Inhalation Aerosol Due to Defective Valve

    Teva Pharmaceuticals is recalling QVAR inhalation aerosol canisters because the delivery system and valve are defective.

    Product
    QVAR¿ (beclomethasone dipropionate HFA), 80mcg Inhalation Aerosol, 50 metered inhalations/120 metered inhalations, packaged in an aluminum cylinder, Mktd. by: Teva Respiratory, LLC, Horsham, PA, Mfd. by: 3M Drug Delivery Systems, Northridge, CA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1751-2013·2013-07-24

    Hospira Recalls Symbiq IV Pump Sets Due to Air-in-Line Alarm Risk

    Hospira is recalling Symbiq IV pump sets because a defective ball valve may fail to seal, causing air-in-line alarms during fluid administration.

    Product
    LifeShield; Sterile; Rx only; List No. 19666-28; SYMBIQ PUMP SET, CONVERTIBLE PIN, PIGGYBACK, 2 CLAVES PORTS AND OPTION LOK, NON-DEHP; NOMINAL LENGTH: 97 IN (249 CM); PRIMING VOLUME: 14 ML; For the administration of I.V. fluids; Made in Costa Rica; Hospira, Inc., Lake Forest, IL
    Category
    Medical Device
    Distribution
    Distributed nationwide