PlainRecalls

Waldemar Link GmbH & Co. Kg (Mfg Site)

Compiled from official public sources by the publisher.

65 recalls on record · Latest: Aug 19, 2026

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Agency notice ledger

Federal filing book Waldemar Link GmbH MID-BOOK · SINGLE-AGENCY

#282 of 14,151 · 65 notices · 0.062% archive

  • BOOK 65 notices
  • RANK #282 of 14,151
  • SHARE 0.062% archive
  • AGENCY FDA Devices (65)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 19, 2026
  • PHOTO Health Innovations Ph…

Nearest notice-volume peer: Health Innovations Pharmacy, Inc (0 notice gap)

Waldemar Link GmbH & Co. Kg (Mfg Site) accounts for about 0.062% of the 104,423-notice archive on 65 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 →

Waldemar Link GmbH's standing among 14,151 recalling firms

Waldemar Link GmbH & Co. Kg (Mfg Site) ranks 282nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Waldemar Link GmbH vs all firms by recall-notice count

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

65 282nd of 14151 higher than 13,869 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

Waldemar Link GmbH in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Waldemar Link GmbH & Co. Kg (Mfg Site) holds about 0.062% of archive notices alongside 65 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 20 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-120/00
FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 23 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-23/00
FDA Devices Moderate Jul 12, 2023

LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8, Lateral-Right/Medial-Left, 5mm-Intended for primary and revision total knee replacement in skeletally mature patients. Product Code: 880-307/21
FDA Devices Moderate Jul 12, 2023

LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8, Medial-Right/Lateral Left, 5mm- Intended for primary and revision total knee replacement in skeletally mature patients. Product Code: 880-307/11
FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left
FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right
FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right
FDA Devices Moderate Jul 20, 2022

Tibial Component Modular. orthopedic prosthesis. Model Nos: Small, W 16-2817/32 Medium, W 16-2817/35 Large, W 16-2817/37
FDA Devices Moderate Jul 20, 2022

Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No #15-2814/04). orthopedic prosthesis.
FDA Devices Moderate Jul 20, 2022

Endo Model Modular Femur and Tibia, PorEx. orthopedic prosthesis. Model Nos.: X-Small, Right 15-3815/11, Small, Right 15-3816/11, Small, Left 15-3816/12, Medium, Right 15-3817/11, Medium, Left 15-3817/12, Large, Right 15-3818/11.
FDA Devices Moderate Jul 20, 2022

Tibial Component. orthopedic prosthesis. Model Nos: Small, W 16-2817/02 Medium, W 16-2817/05 Large, W 16-2817/07
FDA Devices Moderate Jan 23, 2019

LINK STEM with Microporous Surface MP Reconstruction Prosthesis, CEMENTLESS (Size XS-0, D: 12mm, L: 160mm), Reference Number 172-916/12 Product Usage: The LINK¿ STEM with Microporous Surface MP¿ Reconstruction Prosthesis, CEMENTLESS System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The LINK¿ STEM with Microporous Surface MP¿ Reconstruction Prosthesis, CEMENTLESS System is indicated for

FDA Devices Moderate Jan 23, 2019

BiMobile UHMWPE Liner: ID-28mm/OD-54mm, Reference Number 184-260/04 The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intended for cemented and cementless use.
FDA Devices Moderate Jan 23, 2019

BiMobile UHMWPE Liner: ID-28mm/OD-50mm, Reference Number 184-260/02 The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intended for cemented and cementless use.

Waldemar Link GmbH carries an outsized archive share

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.

Philips Medical Systems, Inc. 65 Stryker Sustainability Solutions 65 Microbiologics Inc 66 Nobel Biocare Usa Llc 66

Frequently Asked Questions

How many federal recall notices name Waldemar Link GmbH? ▼
PlainRecalls indexes 65 distinct federal recall events naming Waldemar Link GmbH & Co. Kg (Mfg Site), 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 Waldemar Link GmbH sit among other recalling firms? ▼
Waldemar Link GmbH & Co. Kg (Mfg Site) ranks #282 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Waldemar Link GmbH's notices? ▼
FDA Devices accounts for 65 of this firm's 65 indexed notices.
What product category dominates Waldemar Link GmbH's filing book? ▼
Filings for Waldemar Link GmbH & Co. Kg (Mfg Site) 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.
Waldemar Link GmbH & Co. Kg (Mfg Site): 65 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 Waldemar Link GmbH & Co. Kg (Mfg Site); individual notices remain authoritative on each linked recall page.

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