The Recall Desk

Manufacturer

Mckesson

4 recalls in our database name Mckesson as the manufacturing or recalling firm.

What the numbers show

Total
4
Critical
1
Severe
0
Most recent
2026-07-08

Of the 4 recalls from Mckesson we have scored against our rubric, 1 (25%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–4 of 4

  • ModerateFDA (Drugs)·D-0714-2026·2026-07-08

    Gemcitabine Injection Recalled Due to Temperature Storage Abuse

    McKesson is recalling Gemcitabine Injection (1 g per 26.3 mL) due to temperature abuse—the product was stored at controlled room temperature instead of under refrigeration. The affected lot was distributed nationwide.

    Product
    GEMCITABINE — GEMCITABINE (GEMCITABINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0353-2026·2026-02-18

    UDENYCA syringes recalled after cartons were stored at room temperature

    McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.

    Product
    UDENYCA — UDENYCA (PEGFILGRASTIM-CBQV)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0005-2015·2014-10-15

    Mylan Amiodarone Hydrochloride Injection Recalled for Temperature Abuse

    Mylan Institutional LLC is recalling Amiodarone HCl Injection due to inadvertent refrigeration during distribution. McKesson distributed the affected vials to facilities in WA, OR, and MT.

    Product
    AMIODARONE HYDROCHLORIDE — AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    3 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

McKesson Corporation

U.S. healthcare supplies

Country
United States
Founded
1833

Official website

Source: Wikidata (Q570473), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.