PlainRecalls

Fresenius Kabi USA LLC (Fk USA)

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Aug 28, 2013

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Agency notice ledger

Federal filing book Fresenius Kabi USA LLC LIGHT-BOOK · SINGLE-AGENCY

#4,840 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #4,840 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Drug (2)
  • CAT drugs
  • CATS 1 category
  • LATEST Aug 28, 2013
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Fresenius Kabi USA LLC (Fk USA) accounts for about 0.002% of the 104,423-notice archive on 2 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 →

How Fresenius Kabi USA LLC compares to 14,151 recalling firms

Fresenius Kabi USA LLC (Fk USA) ranks 4,840th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Fresenius Kabi USA LLC vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

2 4840th of 14151 higher than 8,037 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

Fresenius Kabi USA LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Fresenius Kabi USA LLC (Fk USA) holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Drug Moderate Aug 28, 2013

IRINOTECAN HYDROCHLORIDE INJECTION, 40 mg/2 mL (20 mg/mL), 2 mL Single Dose Vial, Rx only, Manufactured for: APP Pharmaceuticals, LLC, Schaumburg, IL 60173, NDC 63323-193-02, UPC 3 63323 19302 7.
FDA Drug Low Mar 20, 2013

CALCIUM GLUCONATE INJECTION, USP, 10% (100 mg/mL), 10 mL, Single Dose Vial, Rx only, For Direct Slow IV or IV Additive Use Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- Product Code 31110, NDC 63323-311-10

Fresenius Kabi USA LLC is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Fresenius Kabi USA LLC? ▼
PlainRecalls indexes 2 distinct federal recall events naming Fresenius Kabi USA LLC (Fk USA), aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Fresenius Kabi USA LLC sit among other recalling firms? ▼
Fresenius Kabi USA LLC (Fk USA) ranks #4,840 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Fresenius Kabi USA LLC's notices? ▼
FDA Drug accounts for 2 of this firm's 2 indexed notices.
What product category dominates Fresenius Kabi USA LLC's filing book? ▼
Filings for Fresenius Kabi USA LLC (Fk USA) span 1 product category, led by drugs. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Fresenius Kabi USA LLC (Fk USA): 2 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Drug). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Fresenius Kabi USA LLC (Fk USA); individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026