Zimmer GmbH
99 recalls on record · Latest: Sep 18, 2024
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Agency notice ledger
Federal filing book Zimmer GmbH MID-BOOK · SINGLE-AGENCY
#170 of 14,151 · 99 notices · 0.095% archive
- BOOK 99 notices
- RANK #170 of 14,151
- SHARE 0.095% archive
- AGENCY FDA Devices (99)
- CAT medical devices
- CATS 1 category
- LATEST Sep 18, 2024
- PHOTO Advanced Pharma Inc.
Nearest notice-volume peer: Advanced Pharma Inc. (0 notice gap)
Zimmer GmbH accounts for about 0.095% of the 104,423-notice archive on 99 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 Zimmer GmbH compares to 14,151 recalling firms
Zimmer GmbH ranks 170th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Zimmer GmbH vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
99 170th of 14151 higher than 13,981 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
Zimmer GmbH in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Zimmer GmbH (this)
Zimmer GmbH
99 notices
- Advanced Phar…
Advanced Pharma Inc.
99 notices
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99 notices
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99 notices
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Fresh Express Incorporated
99 notices
- Kenworth
Kenworth
99 notices
What this shows Zimmer GmbH holds about 0.095% of archive notices alongside 99 distinct filings.
FDA Devices Moderate May 29, 2019
Drill, 15mm stop, 1x76mm, AO , Item Number 502015115
FDA Devices Moderate May 29, 2019
Drill, cannulated, 4x150mm, AO, Item Number ST502015403
FDA Devices Moderate May 29, 2019
CBS micro, countersink, cannulated, AO, Item Number ST503004541
FDA Devices Moderate May 29, 2019
Drill, cannulated, 3x90mm, round shaft, Item Number ST502015630
FDA Devices Moderate May 29, 2019
Drill, 26mm stop, 1.9x94mm, Stryker, Item Number 502015130
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number 502015206
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207
FDA Devices Moderate May 29, 2019
V-TEK", Micro-countersink, AO , Item Number ST28.66.113
FDA Devices Moderate May 29, 2019
V-TEK", standard-countersink, cannulated, AO, Item Number ST28.66.111
FDA Devices Moderate May 29, 2019
Drill, cannulated, 4x120mm, AO, Item Number 502015402
FDA Devices Moderate May 29, 2019
V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, contra-angle, Item Number 502015634
FDA Devices Moderate May 29, 2019
Drill, cannulated, 2.5x95mm, round shaft, Item Number 502015620
FDA Devices Moderate May 29, 2019
MaxiCan 4.5 countersink, cannulated, AO, Item Number 503004177
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 2x125mm, Stryker, Item Number 502015211
FDA Devices Moderate May 29, 2019
Drill, 2.7x125mm, AO , Item Number ST502015217
FDA Devices Moderate May 29, 2019
Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015146
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number ST502015206
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 2x100mm, AO, Item Number ST502015208
FDA Devices Moderate May 29, 2019
CBS high, countersink, cannulated, AO, Item Number 503004542
FDA Devices Moderate May 29, 2019
CBS high, countersink, cannulated, AO, Item Number ST503004542
FDA Devices Moderate May 29, 2019
Drill, 3.2x145mm, AO, Item Number 502015650
FDA Devices Moderate May 29, 2019
V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, AO, Item Number 502015636
FDA Devices Moderate May 29, 2019
V-TEK", standard-countersink, cannulated, round shaft, Item Number 28.66.110
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 2x120mm, AO, Item Number ST502015212
FDA Devices Moderate May 29, 2019
Drill for 2.7mm screw, 2x100mm, AO, Item Number 502015208
FDA Devices Moderate May 29, 2019
Drill for 3.5mm screw, 2.5x125mm, stryker, Item Number 502015218
FDA Devices Moderate May 29, 2019
CBS 4.0 countersink, cannulated, 30mm stop, AO, Item Number 503004353
FDA Devices Moderate May 29, 2019
Drill, cannulated, 2.5x95mm, round shaft, Item Number ST502015620
FDA Devices Moderate May 29, 2019
Drill, 2.7x125mm, AO, Item Number 502015217
FDA Devices Moderate May 29, 2019
Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015124
FDA Devices Moderate May 29, 2019
Drill, cannulated, 4x150mm, AO, Item Number 502015403
FDA Devices Moderate Dec 26, 2018
Avenir¿ Muller Stem Standard, uncemented HA, 1, Taper 12/14 Item Number: 01.06010.001 - Product Usage: Avenir@ Muller Stems are intended to reduce pain and increase hip mobility through long term cementless fixation of total or hemi hip arthroplasty in the femur of patients with an adequate bone stock to support the component. A system consisting of a stem, a ball head and a cup is used for the treatment of degenerative diseases or trauma of the hip. All Avenir Muller Stems are intended to provi
FDA Devices Moderate May 2, 2018
Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496
FDA Devices Moderate May 2, 2018
Avenir Muller Stem; Item Number: 01.06010.003, Lot Number: 2904368, UDI: (01) 00889024479494 (17) 220331 (10) 2904368
FDA Devices Moderate Apr 18, 2018
Normed Charcot Osteotome Chisel (Various sizes)
FDA Devices Moderate May 24, 2017
Normed General Instruments 503004541: Werber Countersink Cannulated for micro CBS Screws, AO 503004341: Werber Countersink Cannulated for micro CBS Screws, round-shaft The Countersink is an instrument which is used over the guide wire to prepare for adequate space in the cortical bone rim to sink the screw head in to bones/tissues for different Foot, Ankle and Hand implant systems. The instrument is used in several Normed implant systems. The instrument is used to avoid soft tissue irritation
FDA Devices Moderate Aug 10, 2016
V-TEK TWIST D 3.5X90MM 30MM Can 12MM Rnd; The twist drill is used to drill holes into bones/tissues for foot, ankle and hand implant systems.
FDA Devices Moderate Aug 10, 2016
V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd; The twist drill is used to drill holes into bones/tissues for foot, ankle and hand implant systems.
FDA Devices Moderate Aug 10, 2016
TWIST DR 25X95MM Cann 12MM Thd 30MM AO; The twist drill is used to drill holes into bones/tissues for foot, ankle and hand implant systems.
FDA Devices Moderate Aug 10, 2016
TWIST D 28X150MM CBS 45 Cann 14 MM AO; The twist drill is used to drill holes into bones/tissues for foot, ankle and hand implant systems.
FDA Devices Moderate Aug 3, 2016
Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis Intended Use: " Advanced wear of the joint due to degenerative, post-traumatic or rheumatic diseases. " Failed previous hip surgery including joint reconstruction (osteotomy), arthrodesis, hemiarthroplasty or total hip replacement (THR). " Acute traumatic fracture of the femoral head or neck " Avascular necrosis of the femoral head. " Aveni
FDA Devices Moderate Jun 22, 2016
Dome Centric component (Reference 01.04227.005) from the Anatomical Shoulder (AS) System 2.0. The Dome Centric connects the Humeral Stem to the Humeral Head and allows setting an inclination and retroversion positioning. The Anatomical Shoulder System is intended for long-term implantation into the human shoulder joint in primary or revision, total or hemi shoulder arthroplasty. The system is intended to relieve pain and restore function in patients with adequate bone stock to support the pros
FDA Devices Moderate Oct 21, 2015
Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone.
FDA Devices Moderate May 6, 2015
Anatomical Shoulder Handle for Rasp Item: 01.04233.000 Used during total joint arthroplasty of the shoulder.
FDA Devices Moderate Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of the proximal femur in total hip arthroplasty.
FDA Devices Moderate Mar 4, 2015
Metasul Femoral Head - indicated for total hip arthroplasty for treatment of patient conditions of non-inflammatory degenerative joint disease.
FDA Devices Moderate Mar 4, 2015
Metasul Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of the proximal femur in total hip arthroplasty.
FDA Devices Moderate Mar 4, 2015
CoCr Femoral Head - indicated for hip arthroplasty for noncemented use in skeletally mature invididuals undergoing primary surgery for rehabilitating hips damaged as a result of noninflammatory degenerative joint disease
FDA Devices Moderate Mar 4, 2015
Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Head is used in conjunction with compatible acetabular and femoral stem components in total hip arthroplasty. A variety of sizes and neck lengths are available for various patient anatomies and adjustment of the tension of the ligaments and reconstruction of the center of the natural head of the femur.
Zimmer GmbH carries an outsized archive share
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 (99 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Zimmer GmbH? ▼
PlainRecalls indexes 99 distinct federal recall events naming Zimmer GmbH, 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 GmbH sit among other recalling firms? ▼
Zimmer GmbH ranks #170 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 GmbH's notices? ▼
FDA Devices accounts for 99 of this firm's 99 indexed notices.
What product category dominates Zimmer GmbH's filing book? ▼
Filings for Zimmer GmbH 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 GmbH: 99 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 GmbH; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026