The Recall Desk

FDA (Drugs) recall action 93681

Pfizer Inc. recalled 3 products on 2024-01-24

The FDA (Drugs) publishes a recall like this one as 3 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 3 pages.

Products
3
Announced
2024-01-24
Critical
0
Units
79,600

Why these products were recalled

Presence of Particulate Matter; identified as glass

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–3 of 3

  • SevereFDA (Drugs)··2024-01-24

    Sodium Bicarbonate Injection recalled for glass particulate contamination

    Pfizer is recalling 34,000 cartons of 4.2% Sodium Bicarbonate Injection nationwide due to glass particles in the solution. Patients should immediately stop use and contact their supplier.

    Product
    4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).
    Category
    Distribution
    1 state
  • SevereFDA (Drugs)··2024-01-24

    FDA Recalls Sodium Bicarbonate Injection Due to Glass Particle Contamination

    Pfizer Inc. is recalling 21,200 cartons of Sodium Bicarbonate Injection (lot HA7295, expiring March 1, 2025) nationwide due to glass particle contamination. The product is distributed in the United States and Puerto Rico.

    Product
    SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Distribution
    1 state
  • SevereFDA (Drugs)··2024-01-24

    Atropine Sulfate Injection Recalled for Glass Particulate Matter Contamination

    Pfizer Inc. is recalling Atropine Sulfate Injection due to glass particulate matter contamination in lot GY2496. This FDA Class I recall affects 24,400 cartons distributed nationwide in the USA and Puerto Rico.

    Product
    ATROPINE SULFATE (ATROPINE SULFATE)
    Category
    Distribution
    1 state