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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94681

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

Open FDA event record

Event summary

Timeline bucket
May 20, 2024
Product types
Drug
Classifications
Class II
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

2 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 2

Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intramuscular or Intravenous Use, Rx Only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-2012-03

D-0564-2024
Recall number
D-0564-2024
Initiated
May 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Pfizer Inc.
Quantity
84,710 cartridges

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility-The potential for incomplete crimp seals.

Code information

Lot#: HJ3965; Exp 2024/09 Lot#: HJ8546; Exp 2024/10

Distribution pattern

US Nationwide and Puerto Rico.

drug · product 2 of 2

Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intravenous Injection Only, Rx Only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-2339-24

D-0565-2024
Recall number
D-0565-2024
Initiated
May 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Pfizer Inc.
Quantity
220,400 cartridges

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility-The potential for incomplete crimp seals.

Code information

Lot#: HJ7566; Exp 2025/05 Lot#: HN8747; Exp 2025/09 Lot#: HN8749; Exp 2025/09

Distribution pattern

US Nationwide and Puerto Rico.