The Recall Desk

Hazard

Glass Particles recalls

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

What the numbers show

Total
45
Critical
1
Severe
14
Most recent
2026-09-02

Of the 45 glass particles recalls we have scored against our rubric, 1 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 14 (31%) 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 glass particles 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.

26–45 of 45

  • HighFDA (Devices)·Z-2062-2017·2017-05-17

    Abbott Recalls Healon Medical Device Due to Glass Particle Risk

    Abbott Medical Optics is recalling Healon medical devices because certain lots may contain microscopic glass particles from manufacturing damage.

    Product
    Healon, Part No. 10290953, 10295210, 10200011, 10200012, 10201012, 10203012, 10213012, 10223012, 10290701, 10294751, 10295701
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2063-2017·2017-05-17

    Abbott Recalls Healon GV Due to Possible Microscopic Glass Particles

    Abbott Medical Optics is recalling Healon GV due to a remote possibility of microscopic glass particles from manufacturing damage.

    Product
    Healon GV, Part No. 10294701, 10294801, 10200014, 10201014, 10202014, 10203014
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2066-2017·2017-05-17

    Abbott Recalls Healon Pro Due to Possible Glass Particles

    Abbott Medical Optics is recalling Healon Pro ophthalmic solutions because manufacturing damage may have introduced microscopic glass particles.

    Product
    Healon Pro, Part No. 10270012
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2064-2017·2017-05-17

    Abbott Recalls Healon Duet Due to Potential Glass Particles

    Abbott Medical Optics is recalling Healon Duet units because they may contain microscopic glass particles from manufacturing damage.

    Product
    Healon Duet, Part No. 10290080, 10220010, 10220011 and 10220012
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2785-2016·2016-09-21

    Allergy Laboratories Recalls Sterile Empty Vials Due to Glass Particles

    Allergy Laboratories is recalling 81,625 sterile empty vials distributed in North Carolina due to a potential for glass particles within the vials.

    Product
    GREER 2 ML Sterile Empty Vials 2-13 vial 25 ea - Silver Cap
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2537-2016·2016-08-31

    Cook Inc. Recalls Roadrunner Uniglide Hydrophilic Wire Guides Due to Glass Contamination

    Cook Inc. is recalling Roadrunner Uniglide Hydrophilic Wire Guides because they may be contaminated with glass particles. The recall covers 8,750 devices distributed worldwide.

    Product
    Roadrunner Uniglide Hydrophilic Wire Guide, Catalog Numbers and GPN: HPWA-18-260, G30489; HPWA-18-320, G30490; HPWA-25-260, G30491; HPWA-35-260, G30492; HPWAS-35-260, G30506; HPW-35-150, G56149; HPW-35-180, G56150; HPWS-35-150, G56152; HPWS-35-180, G56153; HPWA-35-80, G56172; HPW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0503-2016·2016-01-20

    Nestle Recalls Sweet Leaf Lemonade Tea Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Half and Half Lemonade Tea because the product contains glass particles.

    Product
    Sweet Leaf Organic Half and Half Lemonade Tea, 16 oz glass bottle UPC: 6-51538-06708-1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2016·2016-01-20

    Sweet Leaf Organic Raspberry Iced Tea Recalled for Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Raspberry Iced Tea because the product contains glass particles.

    Product
    Sweet Leaf Organic Raspberry Iced Tea, 16 oz glass bottle UPC: 6-51538-06703-6
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0506-2016·2016-01-20

    Nestle Recalls Sweet Leaf Peach Iced Tea Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf All Natural Peach Iced Tea because the product contains glass particles.

    Product
    Sweet Leaf All Natural Peach Iced Tea , 16 oz glass bottle UPC: 6-51538-06704-3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0507-2016·2016-01-20

    Nestle Recalls Sweet Leaf Organic Tea Mint & Honey Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Tea Mint & Honey because the product contains glass particles.

    Product
    Sweet Leaf Organic Tea Mint & Honey, 16 oz glass bottle UPC: 6-51538-06701-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0505-2016·2016-01-20

    Nestle Recalls Sweet Leaf Citrus Green Tea Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf All Natural Citrus Green Tea because the product contains glass particles.

    Product
    Sweet Leaf All Natural Citrus Green Tea, 16 oz glass bottle UPC: 6-51538-06720-3
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0297-2015·2014-12-17

    Fresenius Kabi Recalls Cyanocobalamin Vials Due to Sterility Concerns

    Fresenius Kabi USA is recalling 240,550 vials of Cyanocobalamin Injection due to potential glass fractures and particles that compromise sterility.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0296-2015·2014-12-17

    FDA Recalls Ondansetron Injection Vials Due to Sterility Concerns

    Fresenius Kabi USA is recalling 184,550 vials of Ondansetron Injection due to potential glass fractures and particles that compromise sterility.

    Product
    ONDANSETRON — ONDANSETRON (ONDANSETRON HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1747-2013·2013-07-24

    Staar Surgical Recalls Intraocular Lenses Due to Glass Particles

    Staar Surgical is recalling specific Afinity and nanoFLEX intraocular lenses because glass particles may be present in the storage vials.

    Product
    Afinity CQ2015A Intraocular Lens The visual correction of aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by cataract extraction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1746-2013·2013-07-24

    Staar Surgical Recalls Intraocular Lenses Due to Glass Particles

    Staar Surgical is recalling nanoFLEX and Afinity intraocular lenses because glass particles may be present in the storage vials.

    Product
    nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by cataract extraction. The IOL is to be implanted in the posterior chamber and in the capsular bag through a tearfree capsulorhexis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1679-2012·2012-09-26

    Hospira Recalls Carboplatin Injection Due to Embedded Glass Particles

    Hospira Inc. is recalling Carboplatin Injection vials because visible particles are embedded in the glass neck, posing a risk of dislodging into the solution.

    Product
    CARBOPLATIN — CARBOPLATIN (CARBOPLATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1681-2012·2012-09-26

    Hospira Recalls Methotrexate Injection Due to Embedded Glass Particles

    Hospira Inc. is recalling Methotrexate Injection vials because visible particles embedded in the glass neck may dislodge into the solution.

    Product
    METHOTREXATE — METHOTREXATE (METHOTREXATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1682-2012·2012-09-26

    Hospira Recalls Paclitaxel Injection Due to Embedded Glass Particles

    Hospira Inc. is recalling Paclitaxel Injection vials because visible particles are embedded in the glass at the neck. The particles may dislodge into the solution.

    Product
    PACLITAXEL — PACLITAXEL (PACLITAXEL)
    Category
    Drug
    Distribution
    Distributed nationwide