PFIZER INC.
3 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (3)
Registered facilities (6)
- Pfizer Manufacturing Belgium NV FEI 1000654629 · BE
- Wyeth Pharmaceuticals LLC FEI 3004393730 · PA
- Pfizer Inc FEI 3004945409 · NJ
- HOSPIRA, INC. FEI 1925262 · KS
- PHARMACIA & UPJOHN COMPANY LLC FEI 1810189 · MI
- Pfizer Service Company BV FEI 3002522469 · BE
Recalls & enforcement
- Class IITerminated2018-10-02The firm received complaints of the wrap coming apart and leaking granular material
- Class IITerminated2016-12-30Depleted Battery alarm shows instead of Replace Battery. On battery power, ongoing therapy stops, alarms show and sound, pump shuts down after 3 minutes. On AC power, the pump reboots (takes about 25 seconds). Therapy can resume. AC power interruption of 3-7 seconds prompts an …
- Class IITerminated2016-07-28Hospira MedNet 6.1 software, in combination with the SapphirePlus 13.1x infusion pump, may result in incorrect bolus amount calculations for drugs whose concentrations are listed in Million Units.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “PFIZER INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9924008-pfizer-inc/
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