PlainRecalls

Zimmer Biomet, Inc.

Compiled from official public sources by the publisher.

875 recalls on record · Latest: Dec 30, 2020

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Agency notice ledger

Federal filing book Zimmer Biomet, Inc. HEAVY-BOOK · SINGLE-AGENCY

#1 of 14,151 · 875 notices · 0.838% archive

  • BOOK 875 notices
  • RANK #1 of 14,151
  • SHARE 0.838% archive
  • AGENCY FDA Devices (875)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 30, 2020
  • PHOTO Medline Industries, LP

Nearest notice-volume peer: Medline Industries, LP - Northfield (53 notice gap)

Zimmer Biomet, Inc. sits #1 of 14,151 (1st among 14,151 firms) with 875 federal notices — about 0.838% of the archive (heavy-book tercile). Rank counts issuance frequency, not danger. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Zimmer Biomet, Inc. compares to 14,151 recalling firms

Zimmer Biomet, Inc. ranks 1st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Zimmer Biomet, Inc. vs all firms by recall-notice count

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

875 1st of 14151 the highest 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

Zimmer Biomet, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Zimmer Biomet, Inc. carries 875 distinct federal notices, ranked #1 of 14,151 (heavy-book).

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 440MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 420MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 13MM X 320MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 280MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 440MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 360MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 11MM X 320MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 320MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 400MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 13MM X 460MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 260MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 260MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, 125 DEG 9MM X 180MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 440MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 420MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 400MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 320MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 300MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 340MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 13MM X 280MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 300MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 340MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 11MM X 380MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 300MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 420MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 340MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 440MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 360MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 9MM X 260MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 11MM X 300MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 420MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 380MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 13MM X 300MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 280MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 13MM X 260MM
FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 420MM
FDA Devices Moderate Jan 24, 2018

Persona Partial Knee System, Size 8, Finishing Guide
FDA Devices Moderate Jan 10, 2018

RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817
FDA Devices Moderate Jan 10, 2018

CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064
FDA Devices Moderate Jan 10, 2018

Lateral Troch Plate Full Crimp - 254mm, model # 350838
FDA Devices Moderate Jan 10, 2018

PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended to replace the natural acetabulurn damaged by disease, trauma or revision of previous arthroplasty. The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended for uncemented use only.
FDA Devices Moderate Jan 10, 2018

COMP 12MM HUM FRAC STEM MACRO, model # 11-113562
FDA Devices Moderate Jan 10, 2018

OSS CEMENTED IM STEM 12X150, model # 150366
FDA Devices Moderate Jan 10, 2018

RED SEXP DSTL FEM 19CM LT ASSY, model # CP111828
FDA Devices Moderate Jan 10, 2018

COMP PRIMARY STEM 8MM MINI, model # 113628
FDA Devices Moderate Jan 10, 2018

CER BIOLOXD OPTION HD 32MM, model # 650-1056
FDA Devices Moderate Jan 10, 2018

Lateral Troch Plate Full Crimp - 254mm, model # 350837
FDA Devices Moderate Jan 10, 2018

ECHO POR FMRL NC 9X125, model # 192009
FDA Devices Moderate Dec 27, 2017

ExploR Radial Head Replacement System. PN: 11-210061 LN: 243610. The stem is placed inside a polyurethane bag. The bagged component will then be placed in an inner PETG tray. The screw will be placed inside a separate polybag, and placed in the PETG tray with foam pieces added to the top and bottom of the tray for protection. The inner tray and the contents within will then have a Tyvek¿ lid heat sealed to the tray. The sealed inner tray will be fit into an outer PETG tray and a Tyvek¿ lid he
FDA Devices Moderate Dec 6, 2017

ROSA Surgical Device 2.5.8

Zimmer Biomet, Inc. sits in the heavy federal notice book

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 Zimmer Biomet, Inc.? ▼
PlainRecalls indexes 875 distinct federal recall events naming Zimmer Biomet, 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 Zimmer Biomet, Inc. sit among other recalling firms? ▼
Zimmer Biomet, Inc. ranks #1 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 Zimmer Biomet, Inc.'s notices? ▼
FDA Devices accounts for 875 of this firm's 875 indexed notices.
What product category dominates Zimmer Biomet, Inc.'s filing book? ▼
Filings for Zimmer Biomet, 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.
Zimmer Biomet, Inc.: 875 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 Zimmer Biomet, Inc.; individual notices remain authoritative on each linked recall page.

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