The Recall Desk

Hazard

Particulate Matter recalls

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

What the numbers show

Total
410
Critical
57
Severe
186
Most recent
2026-09-02

Of the 410 particulate matter recalls we have scored against our rubric, 57 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 186 (45%) 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 particulate matter 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.

401–410 of 410

  • SevereFDA (Drugs)·D-1697-2012·2012-10-03

    Ben Venue Recalls Vecuronium Bromide Injection Due to Particulate Matter

    Ben Venue Laboratories is recalling Vecuronium Bromide for Injection due to the presence of particulate matter.

    Product
    Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr. By: Ben Venue Laboratories, Bedford, OH 44146: Mfg for: Bedford Labs, Bedford, OH 44146, NDC 55390-039-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1685-2012·2012-10-03

    Hospira Recalls Propofol Injectable Emulsion Due to Particulate Matter

    Hospira Inc. is recalling 148,630 vials of Propofol Injectable Emulsion because a single visible particulate was found in sample bottles during inspection.

    Product
    PROPOFOL — PROPOFOL (PROPOFOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1439-2012·2012-08-08

    Apotex Recalls Dorzolamide HCI/Timolol Maleate Ophthalmic Solution Due to Particulates

    Apotex Inc. is recalling specific lots of Dorzolamide HCI/Timolol Maleate Ophthalmic Solution because they may contain small particulates.

    Product
    Dorzolamide HCI/Timolol Maleate Ophthalmic Solution 22.3mg/6.8mg per mL, 10mL bottle, For Topical Application in the Eye, Sterile Ophthalmic Solution, Rx Only, Mfg by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1437-2012·2012-08-08

    West-Ward Recalls Fosphenytoin Sodium Injection Due to Particulate Matter

    West-Ward Pharmaceutical Corp. is recalling specific lots of Fosphenytoin Sodium Injection because particles were found in stability and retain samples.

    Product
    FOSPHENYTOIN SODIUM — FOSPHENYTOIN SODIUM (FOSPHENYTOIN SODIUM)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1438-2012·2012-08-08

    West-Ward Recalls Fosphenytoin Sodium Injection Due to Particulate Matter

    West-Ward Pharmaceutical Corp. is recalling specific lots of Fosphenytoin Sodium Injection because particles were found in stability and retain samples.

    Product
    FOSPHENYTOIN SODIUM — FOSPHENYTOIN SODIUM (FOSPHENYTOIN SODIUM)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1432-2012·2012-08-08

    Cadence Pharmaceuticals Recalls OFIRMEV Acetaminophen Injection Due to Particulate Matter

    Cadence Pharmaceuticals is recalling OFIRMEV (acetaminophen) injection vials due to the visible presence of particulate matter.

    Product
    OFIRMEV (acetaminophen) injection, 1000 mg/100 mL (10 mg/mL), 24-count Single Use 100 mL Vials per carton, Rx only, Manufactured for: Cadence Pharmaceuticals, Inc., San Diego, CA 92130, NDC 43825-102-01, UPC 3 43825 10201 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1421-2012·2012-07-25

    Luitpold Recalls Epinephrine Injection Ampules Due to Particulate Matter

    Luitpold Pharmaceuticals is recalling Epinephrine Injection ampules because of the presence of particulate matter. The affected lot was distributed nationwide.

    Product
    Epinephrine Injection, USP, 1:1000 (1 mg/mL), 25 x 1 mL Ampules, For SC and IM Use, For IV and IC Use after Dilution, Rx Only, American Regent, Inc., Shirely, NY 11967 --NDC 0517-1071-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1378-2012·2012-06-20

    Luitpold Recalls Concentrated Sodium Chloride Injection Due to Particulate Matter

    Luitpold Pharmaceuticals is recalling concentrated sodium chloride injection vials because visual particles were found in retention samples.

    Product
    CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE DOSE VIAL, (NDC 0517-2930-25), b) 100 mL PHARMACY BULK PACKAGE (NDC 0517-2900-25), Rx Only, AMERICAN REGENT, INC. SHIRLEY, NY 11967.
    Category
    Drug
    Distribution
    Distributed nationwide