PlainRecalls

DePuy Orthopaedics, Inc.

155 recalls on record · Latest: Apr 10, 2024

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Agency notice ledger

Federal filing book DePuy Orthopaedics, Inc. HEAVY-BOOK · SINGLE-AGENCY

#102 of 14,151 · 155 notices · 0.148% archive

  • BOOK 155 notices
  • RANK #102 of 14,151
  • SHARE 0.148% archive
  • AGENCY FDA Devices (155)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 10, 2024
  • PHOTO Dodge

Nearest notice-volume peer: Dodge (2 notice gap)

DePuy Orthopaedics, Inc. accounts for about 0.148% of the 104,423-notice archive on 155 distinct filings — a heavy 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 DePuy Orthopaedics, Inc. compares to 14,151 recalling firms

DePuy Orthopaedics, Inc. ranks 102nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

DePuy Orthopaedics, Inc. vs all firms by recall-notice count

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

155 102nd of 14151 higher than 14,049 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 · 2026-09-13

DePuy Orthopaedics, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows DePuy Orthopaedics, Inc. holds about 0.148% of archive notices alongside 155 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ5 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foam protectors were in direct contact with the stem to help immobilize the product within the package. The sterile barrier system was then packed within a carton and shrink wrapped. Intended Use: The ULTIMA LX Cemented Polished Femoral Hip Stems product are forged CoCr polished cemented stems which are used as part of a total hip arthroplasty. The

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ2 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foam protectors were in direct contact with the stem to help immobilize the product within the package. The sterile barrier system was then packed within a carton and shrink wrapped. Intended Use: The ULTIMA LX Cemented Polished Femoral Hip Stems product are forged CoCr polished cemented stems which are used as part of a total hip arthroplasty. The

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 8 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were packaged within vinyl protectors, with foam taper protectors. Intended Use: The LUSTER Cemented Polished Femoral Hip Stems product are forged CoCr polished cemented stems which are used as part of a total hip arthroplasty. These stems were indicated for use with all DePuy bearings and acetabular cups.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/3M Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foam protectors were in direct contact with the stem to help immobilize the product within the package. The sterile barrier system was then packed within a carton and shrink wrapped. Intended Use: The ULTIMA LX Cemented Polished Femoral Hip Stems product are forged CoCr polished cemented stems which are used as part of a total hip arthroplasty. Thes

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 2 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were packaged within vinyl protectors, with foam taper protectors. Intended Use: The LUSTER Cemented Polished Femoral Hip Stems product are forged CoCr polished cemented stems which are used as part of a total hip arthroplasty. These stems were indicated for use with all DePuy bearings and acetabular cups.

DePuy Orthopaedics, Inc. carries an outsized archive share

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 DePuy Orthopaedics, Inc.?
PlainRecalls indexes 155 distinct federal recall events naming DePuy Orthopaedics, 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 DePuy Orthopaedics, Inc. sit among other recalling firms?
DePuy Orthopaedics, Inc. ranks #102 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of DePuy Orthopaedics, Inc.'s notices?
FDA Devices accounts for 155 of this firm's 155 indexed notices.
What product category dominates DePuy Orthopaedics, Inc.'s filing book?
Filings for DePuy Orthopaedics, 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.
DePuy Orthopaedics, Inc.: 155 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 DePuy Orthopaedics, Inc.; individual notices remain authoritative on each linked recall page.

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