The Recall Desk

Hazard

Manufacturing Contamination recalls

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

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2024-12-11

Of the 3 manufacturing contamination recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 manufacturing contamination 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.

1–3 of 3

  • HighFDA (Drugs)·D-0099-2025·2024-12-11

    Duloxetine Delayed-Release Capsules Recalled Due to Manufacturing Quality Deviation

    Amerisource Health Services LLC recalls Duloxetine 20 mg delayed-release capsules due to the presence of N-nitroso-duloxetine impurity above acceptable limits. The affected bottles were distributed in Pennsylvania, Ohio, and Puerto Rico.

    Product
    Duloxetine Delayed-Release Capsules, USP, 20 mg, Rx only, 60 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For BluePoint Laboratories NDC 68001-413-06
    Category
    Drug
    Distribution
    3 states
  • HighFDA (Drugs)·D-0772-2023·2023-06-07

    Cough medicine recalled due to manufacturing process deviation with non-food lubricant

    Denison Pharmaceuticals is recalling Safe tussin DM DAY TIME Cough Relief due to use of non-food grade lubricant in the manufacturing process. Approximately 86,616 bottles were distributed nationwide.

    Product
    Safe tussin DM, DAY TIME Cough Relief, (Dextromethorphan HBr, USP 10mg Guaifenesin, USP 100mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1688-2022·2022-09-14

    Thick-It Food & Beverage Thickener recalled for insanitary manufacturing conditions

    Kent Precision Foods Group is recalling Thick-It Original Food & Beverage Thickener due to possible insanitary conditions during manufacturing. The product was distributed to food service facilities including hospitals and nursing homes.

    Product
    Thick-It Original Food & Beverage Thickener 6/36 oz. jars per case
    Category
    Food
    Distribution
    0 states