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.

1–25 of 45

  • SevereFDA (Drugs)·D-0827-2026·2026-09-02

    Fresenius Kabi Recalls Tyenne Injection Due to Glass Particles

    Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.

    Product
    TYENNE — TYENNE (TOCILIZUMAB-AAZG)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0250-2026·2026-01-14

    Intraocular injection syringes recalled over glass-like particulate matter

    Imprimis NJOF is recalling 596 boxes containing 11,920 pre-filled syringes of Dexamethasone, Moxifloxacin and Ketorolac intraocular injection over glass-like particles.

    Product
    Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0251-2026·2026-01-14

    Tri-Moxi intraocular injection recalled over glass-like particulate matter

    Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.

    Product
    Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0249-2026·2026-01-14

    Dexamethasone and moxifloxacin injection recalled over glass-like particulate matter

    Imprimis NJOF is recalling 778 boxes containing 15,540 pre-filled syringes of Dexamethasone and Moxifloxacin intraocular injection over glass-like particles.

    Product
    Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-512-0.1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0413-2025·2025-05-14

    Testosterone Pellet 200 mg Recalled for Glass Particle Contamination

    BSO LLC is recalling compounded testosterone pellets nationwide because glass particles were found in vials. Affected lot numbers are 20250207@1 and 20250228@1 (expiration 1/31/2026).

    Product
    TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0125-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0415-2025·2025-05-14

    Testosterone Pellet 200 mg Recalled Due to Glass Particles

    BSO LLC is recalling Testosterone Pellet 200 mg compounded drug vials nationwide due to the presence of glass particles found in pellet vials.

    Product
    TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0122-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0412-2025·2025-05-14

    Testosterone Pellet 100 mg recalled due to glass particle contamination

    BSO LLC is recalling Testosterone Pellet 100 mg (compounded, office use only) distributed nationwide due to glass particles found in pellet vials.

    Product
    TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0101-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0186-2025·2025-01-15

    Progesterone Injection Recalled Nationwide for Glass Particulate Matter

    Eugia US LLC is recalling Progesterone Injection due to a market complaint of glass particles found in vials. The affected batch poses a potential risk to patients who receive injections from contaminated vials.

    Product
    PROGESTERONE — PROGESTERONE (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0005-2025·2024-10-09

    FDA Recalls Veklury Injection Vials for Presence of Glass Particles

    Gilead Sciences recalls 105,000 vials of Veklury (remdesivir) for injection nationwide because glass particles are present in the medication.

    Product
    VEKLURY — VEKLURY (REMDESIVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0328-2024·2024-02-28

    CVS Health Cherry Cough Drops recalled for potential glass and silicone particles

    Bestco LLC is recalling CVS Health Cherry Cough Drops nationwide due to potential glass and silicone particulates resulting from manufacturing process deviations.

    Product
    CVS Health Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 160 drops per bag, item number 20001089, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0956-2023·2023-06-07

    Trader Joe's Cold Brew Coffee Recalled for Glass Particles

    Trader Joe's Instant Cold Brew Coffee may contain glass particles. Regal Trading is recalling 14,112 cases distributed in eight states. No illnesses have been reported.

    Product
    Trader Joes Instant Cold Brew Coffee, 3.5 oz.(99g), 24 jars per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0305-2023·2023-01-25

    Superior Crunch Salad Mix Recalled for Glass Particle Contamination

    Superior Fresh has recalled Superior Crunch salad mix (4 oz) due to contamination with small glass particles. The affected product was distributed across Indiana, Pennsylvania, Virginia, and Wisconsin.

    Product
    Superior Crunch Net Wt. 4 oz. (113g). Ingredients May Contain Green Leaf, Green Romaine, Green Oak Leaf. Keep Refrigerated. Grown for you By: Superior Fresh LLC, Hixton, WI 54635
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0304-2023·2023-01-25

    Superior Fresh Spring Mix Recalled for Glass Particle Contamination

    Superior Fresh is recalling Spring Mix lettuce products that may contain small glass particles. The affected packages were distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.

    Product
    Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Butter lettuce, Arugula, spinach. Keep Refrigerated. Packaged under the following Names and sizes: 1. Spring Mix Family Pack Net Wt. 8 oz (22
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0302-2023·2023-01-25

    Superior Fresh Lettuce Blend Recalled for Small Glass Particles

    Superior Fresh Lettuce Blend products have been recalled due to the presence of small glass particles. Affected products include Spring Mix, Midwest Medley, and Midwest Medley Family Pack distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.

    Product
    Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Butter lettuce, Arugula, Kale, Spinach, Mustard, Mizuna, Pax Choi. Keep Refrigerated. Packaged under the following Names and sizes: 1. Spring
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0306-2023·2023-01-25

    Superior Fresh Mighty Mix salad recall: glass particle contamination

    Superior Fresh LLC is recalling Mighty Mix salad mix (4 oz packages, Best By 1/23) due to potential contamination with small glass particles. No injuries have been reported; consumers should discard the product.

    Product
    Superior Fresh Mighty Mix, Net Wt. 4 oz. (113g). UPC 8 57871-00883 9. Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Arugula, Mizuna, Pak Choi, Spinach. Keep Refrigerated. Grown for you By: Superior Fresh LLC, Hixt
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0303-2023·2023-01-25

    Superior Fresh Organic Spring Mix Recalled for Glass Particles

    Superior Fresh Organic Spring Mix Family Pack is being recalled due to potential glass particle contamination. The recall affects 1,516 cases distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.

    Product
    Superior Fresh Organic Spring Mix Family Pack. UPC 8 50038-27430 6. Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf. Keep Refrigerated. Grown for you By: Superior Fresh LLC, Hixton, WI 54635
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-0058-2023·2022-11-16

    Octreotide Acetate Injection Recalled for Glass Particle Contamination

    Viatris Inc is recalling Octreotide Acetate Injection due to glass particles found in syringes. Approximately 22,400 syringes of lot #AJ21002 (expiration 03/2024) were distributed nationwide.

    Product
    OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0093-2022·2021-11-10

    Cubicin daptomycin injection recalled for glass particle contamination

    Merck Sharp & Dohme Corp. is recalling Cubicin (daptomycin for injection) 500 mg vials due to the presence of glass particles. The recall affects a single lot distributed nationwide.

    Product
    Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0552-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl and Ropivacaine Bags Due to Particulate Matter

    QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of particulate matter, including potential glass particles.

    Product
    fentaNYL 500 mcg/250 mL (2 mcg/mL) ROPivacaine HCl 0.2% 500 mg/250 mL (2 mg/mL) in 0.9% Sodium Chloride 250 mL Bag Rx, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1225-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0546-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl and Bupivacaine Bags Due to Particulate Matter

    QuVa Pharma is recalling fentanyl and bupivacaine injection bags due to the presence of particulate matter, specifically potential glass particles.

    Product
    fentaNYL 500 mcg/250 mL (2 mcg/mL) Bupivacaine HCl 0.1% 250 mg/250 mL (1 mg/mL) in 0.9% Sodium Chloride 250 mL Bag, Rx only, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1160-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0548-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl and Ropivacaine Infusions Due to Particulate Matter

    QuVa Pharma is recalling specific lots of fentanyl and ropivacaine infusions due to the presence of particulate matter, including potential glass particles.

    Product
    fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200 mg/100 mL (2 mg/mL) in 0.9% Sodium Chloride 100 mL CADD, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478NDC 70092-1259-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0319-2019·2018-12-26

    GE Healthcare Recalls Omnipaque Injection Due to Vial Defect

    GE Healthcare is recalling 1,092 cartons of Omnipaque (iohexol) Injection in Tennessee due to a vial defect that could compromise sterility or introduce glass particles.

    Product
    OMNIPAQUE — OMNIPAQUE (IOHEXOL)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0841-2018·2018-06-13

    Apotex Recalls Fluticasone Propionate Nasal Spray Due to Glass Particles

    Apotex Inc. is recalling Fluticasone Propionate Nasal Spray because glass particles were found in the product. Consumers should stop using the affected lot.

    Product
    FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2065-2017·2017-05-17

    Abbott Recalls Healon 5 Pro Due to Possible Glass Particles

    Abbott Medical Optics is recalling Healon 5 Pro ophthalmic solution because some units may contain microscopic glass particles from manufacturing damage.

    Product
    Healon 5 Pro, Part No. 10270015
    Category
    Medical Device
    Distribution
    0 states