PlainRecalls

Owen Mumford USA, Inc.

Compiled from official public sources by the publisher.

7 recalls on record · Latest: Jul 21, 2021

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Agency notice ledger

Federal filing book Owen Mumford USA, Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,998 of 14,151 · 7 notices · 0.007% archive

  • BOOK 7 notices
  • RANK #1,998 of 14,151
  • SHARE 0.007% archive
  • AGENCY FDA Devices (7)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 21, 2021
  • PHOTO A I Foods Corporation

Nearest notice-volume peer: A I Foods Corporation (0 notice gap)

Owen Mumford USA, Inc. accounts for about 0.007% of the 104,423-notice archive on 7 distinct filings — a mid 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 Owen Mumford USA, Inc. compares to 14,151 recalling firms

Owen Mumford USA, Inc. ranks 1,998th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Owen Mumford USA, Inc. vs all firms by recall-notice count

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

7 1998th of 14151 higher than 12,091 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

Owen Mumford USA, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Owen Mumford USA, Inc. holds about 0.007% of archive notices alongside 7 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 21, 2021

Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
FDA Devices Moderate Nov 13, 2019

Autoject EI, REF AJ1310
FDA Devices Moderate Nov 13, 2019

Petfine Auto Injector, REF 3310VET
FDA Devices Moderate Jan 24, 2018

Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.
FDA Devices Moderate Jan 24, 2018

Unifine Pentips 5mm x 31G pen needles, packaged in 30 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.
FDA Devices Moderate Jul 22, 2015

Autopen Classic Automatic insulin delivery pen, 3.0ml x 2 unit 2-42 units, AN3800, Lot 7JH, NDC 08470-3800-01, The product is a non-sterile automatic subcutaneous injection device which delivers insulin.
FDA Devices Moderate Apr 8, 2015

Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.

Owen Mumford USA, Inc. holds a measurable archive slice

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

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Abbott Diagnostics Scarborough, Inc. 7 Agfa N.v. 7 Alto Development Corp 7 Ambu Inc. 7

Frequently Asked Questions

How many federal recall notices name Owen Mumford USA, Inc.? ▼
PlainRecalls indexes 7 distinct federal recall events naming Owen Mumford USA, Inc., 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 Owen Mumford USA, Inc. sit among other recalling firms? ▼
Owen Mumford USA, Inc. ranks #1,998 of 14,151 by distinct recall-event count among 14,151 firms in this archive (85th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Owen Mumford USA, Inc.'s notices? ▼
FDA Devices accounts for 7 of this firm's 7 indexed notices.
What product category dominates Owen Mumford USA, Inc.'s filing book? ▼
Filings for Owen Mumford USA, Inc. span 1 product category, led by medical devices. 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.
Owen Mumford USA, Inc.: 7 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Owen Mumford USA, Inc.; individual notices remain authoritative on each linked recall page.

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