Hospira a Pfizer Company
4 recalls on record · Latest: Aug 9, 2017
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Agency notice ledger
Federal filing book Hospira a Pfizer Company LIGHT-BOOK · SINGLE-AGENCY
#2,950 of 14,151 · 4 notices · 0.004% archive
- BOOK 4 notices
- RANK #2,950 of 14,151
- SHARE 0.004% archive
- AGENCY FDA Drug (4)
- CAT drugs
- CATS 1 category
- LATEST Aug 9, 2017
- PHOTO 1 Epic, LLC
Nearest notice-volume peer: 1 Epic, LLC (0 notice gap)
Hospira a Pfizer Company accounts for about 0.004% of the 104,423-notice archive on 4 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
Hospira a Pfizer Company's standing among 14,151 recalling firms
Hospira a Pfizer Company ranks 2,950th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Hospira a Pfizer Company vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
4 2950th of 14151 higher than 10,859 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14
Hospira a Pfizer Company in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Hospira a Pfi… (this)
Hospira a Pfizer Company
4 notices
- 1 Epic, LLC
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4 notices
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4 notices
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4 notices
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4 notices
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What this shows Hospira a Pfizer Company holds about 0.004% of archive notices alongside 4 distinct filings.
8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA, NDC: 0409-6625-02
Potassium Phosphates Inj., USP, 45 mM (3 mM P/mL) Also contains: 66 mEq K+ (4.4 mEq/mL) 15 mL, Single-dose, Caution: Must Be Diluted, Rx Only, Mfd by Hospira, Inc. Lake Forest, IL 60045 USA, NDC: 0409-7295-01
Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA
Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.) one vial (NDC: 0409-6629-02), b.) 25 vial carton (NDC: 0409-6629-25).
Hospira a Pfizer Company is a small archive contributor
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (4 here).
Similar drugs volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
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Firm-level totals aggregate distinct federal recall events naming Hospira a Pfizer Company; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026