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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93681

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 21, 2023
Product types
Drug
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
Pfizer Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 3

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).

D-0233-2024
Recall number
D-0233-2024
Initiated
December 21, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Pfizer Inc.
Quantity
34000 Cartons

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
Particulate Matter

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Presence of Particulate Matter; identified as glass

Code information

Lot GX1542, Exp. 01/01/2025

Distribution pattern

Nationwide in the USA and Puerto Rico.

drug · product 2 of 3

8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).

D-0234-2024
Recall number
D-0234-2024
Initiated
December 21, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Pfizer Inc.
Quantity
21200 Cartons

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
Particulate Matter

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Presence of Particulate Matter; identified as glass

Code information

Lot HA7295, EXP 03/01/2025

Distribution pattern

Nationwide in the USA and Puerto Rico.

drug · product 3 of 3

Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake FOrest, IL 60045, NDC 0409-4911-11 (carton), 0409-4911-34 (case).

D-0235-2024
Recall number
D-0235-2024
Initiated
December 21, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Pfizer Inc.
Quantity
24400 Cartons

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
Particulate Matter

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Presence of Particulate Matter; identified as glass

Code information

Lot GY2496, Exp 02/01/2025

Distribution pattern

Nationwide in the USA and Puerto Rico.