U&i Corp.
2 recalls on record · Latest: Jul 29, 2020
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Agency notice ledger
Federal filing book U&i Corp. LIGHT-BOOK · SINGLE-AGENCY
#5,976 of 14,151 · 2 notices · 0.002% archive
- BOOK 2 notices
- RANK #5,976 of 14,151
- SHARE 0.002% archive
- AGENCY FDA Devices (2)
- CAT medical devices
- CATS 1 category
- LATEST Jul 29, 2020
- PHOTO 3M Company
Nearest notice-volume peer: 3M Company (0 notice gap)
U&i Corp. 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 U&i Corp. compares to 14,151 recalling firms
U&i Corp. ranks 5,976th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
U&i Corp. vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
2 5976th 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 · 2026-09-15
U&i Corp. in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- U&i Corp. (this)
U&i Corp.
2 notices
- 3M Company
3M Company
2 notices
- 3M Company
3M Company, of St. Paul, Minn.
2 notices
- 3M Company/3m…
3M Company/3m Espe Dental Products
2 notices
- 3T Design Ltd.
3T Design Ltd., of Hong Kong
2 notices
- A & S Food Tr…
A & S Food Trading Inc.
2 notices
What this shows U&i Corp. holds about 0.002% of archive notices alongside 2 distinct filings.
ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM
Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 - Product Usage:The device is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disk disease at one level from C2-C3 disc to the C7-T1 disc. Each product is composed of four components: PEEK cage, titanium plate, and two titanium markers.
U&i Corp. 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 (2 here).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name U&i Corp.? ▼
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Firm-level totals aggregate distinct federal recall events naming U&i Corp.; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026