The Recall Desk

Hazard

Medication Mixup 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
3
Most recent
2017-12-06

Of the 3 medication mixup recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (100%) 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 medication mixup 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

  • SevereFDA (Drugs)·D-0101-2018·2017-12-06

    Zydus Recalls Paroxetine Tablets Due to Presence of Risperidone

    Zydus Pharmaceuticals is recalling Paroxetine tablets because Risperidone tablets were found in the bottles. Consumers should stop using the affected products.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1141-2015·2015-06-24

    NEXIUM Capsules Recalled Due to Presence of SEROQUEL XR Tablets

    AstraZeneca is recalling NEXIUM capsules because a retail pharmacist found SEROQUEL XR tablets in an unopened bottle.

    Product
    NEXIUM¿ (esomeprazole magnesium), Delayed-Release capsules, 20 mg, 30-count bottle, Rx only, Manufactured for AstraZeneca LLC, Wilmington, Distributed by AstraZeneca, AB, Sodertalje, Sweden. NDC 00186-5020-31.
    Category
    Drug
    Distribution
    Distributed nationwide