PlainRecalls

Zimmer, Inc.

Compiled from official public sources by the editorial team.

440 recalls on record · Latest: May 6, 2026

Zimmer, Inc. Recall Insight

Zimmer, Inc. appears on 440 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.433% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 6, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Nov 20, 2013 to Feb 26, 2014.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Feb 26, 2014

COMPRESSION SCREW (1/2, 1-1/2, 1-1/4, 1-3/4, 1. 2. 3/4 IN)

FDA Devices Moderate Feb 26, 2014

12/14 UNIPOLAR FEMORAL HE VERSYS CEM LD/FX SZ 11X12 VERSYS CEM LD/FX SZ 12X12 VERSYS CEM LD/FX SZ 14X13 VERSYS CEM LD/FX SZ 16X14 VERSYS CEM LD/…

FDA Devices Moderate Feb 26, 2014

TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O TRILOGY ACET SHELL 40MM O TRILOGY ACET SHELL 42MM O TRILOGY ACET SHELL 44MM O TRILOGY ACET S…

FDA Devices Moderate Feb 26, 2014

MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID

FDA Devices Moderate Feb 26, 2014

NEXGEN MIS TIBIA PLATE PR NEXGEN TAPER PLUG NEXGEN PRECOAT PEG TIB PL NEXGEN MICRO ALL-POLY PAT NEXGEN ALL-POLY PATELLA, NEXGEN PRECOAT…

FDA Devices Moderate Feb 26, 2014

HGP II ACETABULAR CUP MOD

FDA Devices Moderate Feb 26, 2014

HGP II ACETABULAR CUP BON

FDA Devices Moderate Feb 26, 2014

6 DEGREE COCR FEM HEAD 36

FDA Devices Moderate Feb 26, 2014

ONE-PIECE LAG SCREW 11MM. Item codes starting with 00225900.

FDA Devices Moderate Feb 26, 2014

VERSA-FX II KEYLESS TUBE, VERSA-FX II KEYLESS SHORT, VERSA-FX II SHORT TUBE PL, VERSA-FX II STD TUBE PLAT and VERSA-FX II SUPRACONDYLR Item codes…

FDA Devices Moderate Feb 26, 2014

I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGII KNEE SLF-TAP BONE ST

FDA Devices Moderate Feb 26, 2014

M/DN R-F IM NAIL 9MM DIA , 10 MM, 11 MM, 12 MM, 13 MM and 14 MM. Item codes starting with 0022400

FDA Devices Moderate Feb 26, 2014

INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some items starting with codes 0022530

FDA Devices Moderate Feb 26, 2014

NEXGEN OSTEOTOMY CORT BON. Item codes starting with 0052500

FDA Devices Moderate Feb 26, 2014

FREE-LOCK LAG SCREW, 12.7, FREE-LOCK LAG SCREW, 15.8, FREE-LOCK SUPRACOND TUBE and FREE-LOCK TUBE & SCP PLAT. Items starting with codes 0011810 and 0…

FDA Devices Moderate Feb 26, 2014

VERSYS HERITAGE FEM STEM

FDA Devices Moderate Feb 26, 2014

6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE

FDA Devices Moderate Feb 26, 2014

ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM, 11 MM, 12 MM, 13 MM, 14 MM and 15 MM) DIA X (18, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48 and 50)

FDA Devices Moderate Feb 26, 2014

HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Items starting with 0011500 and 0011520.

FDA Devices Moderate Feb 26, 2014

FEM HD ION (various sizes)

FDA Devices Moderate Feb 26, 2014

MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFFSET LI

FDA Devices Moderate Feb 26, 2014

Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM, LAG SCR 12.7D X 55 MM SHO up to 100MM, LAG SCR 12.7D X 55MM STAN up to 15…

FDA Devices Moderate Feb 26, 2014

MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001, 455503001 and 455504001

FDA Devices Moderate Feb 26, 2014

MOORE HIP PROS LONG FENES, MOORE HIP PROS NRW STR FE, MOORE HIP PROS STR FENEST, THOMPSON HIP PROSTHESIS sizes 3, 4, 5, and 6, and Mod Austin Moore F…

FDA Devices Moderate Feb 26, 2014

PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM PERI SCR. 3.5MM X 14MM PERI SCR 3.5MM X 44MM STE PERI SCR. 3.5MM X 65MM PERI. SCR 4.0M…

FDA Devices Moderate Jan 29, 2014

Zimmer Segmental Systems; Polyethylene Inserts, Size B. Designed to address significant bone loss resulting from oncology, trauma, and/or salvage …

FDA Devices Moderate Jan 29, 2014

Zimmer Segmental Systems; Polyethylene Inserts, Size C. Knee replacement.

FDA Devices Moderate Jan 22, 2014

Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl Methacrylate Monomer 0.5 g Gen…

FDA Devices Moderate Jan 8, 2014

NGK Stem Ext 24 x 245mm

FDA Devices Moderate Jan 8, 2014

DIST LAT FEM LOCK PLT, RT

FDA Devices Moderate Jan 8, 2014

Versys Build-Up Block The VerSys CRC Hip System is indicated for total hip arthroplasty in patients whose bone stock is of poor quality or inadequ…

FDA Devices Moderate Jan 8, 2014

CPT Hip System, Parts 00-8114-002-10 and 00-8011-004-00 Hip joint metal/polymer semi-constrained cemented prosthesis. The CPT Hip System is indic…

FDA Devices Moderate Jan 8, 2014

FEM COND BUTTRESS PLT, LT

FDA Devices Moderate Jan 8, 2014

TIB NAIL

FDA Devices Moderate Jan 8, 2014

TIBIO FEM/FEM NAIL.

FDA Devices Moderate Jan 8, 2014

Trabecular Metal (TM) Reverse Glenosphere 36mm Part 00-4349-036-11 The reverse shoulder system is used in the treatment of the following: severe…

FDA Devices Moderate Jan 8, 2014

FEM COND BUTTRESS PLT, RT.

FDA Devices Moderate Jan 8, 2014

ITST THREADED GUIDE PIN

FDA Devices Moderate Jan 8, 2014

DIST LAT FEM LOCK PLT, LT

FDA Devices Moderate Dec 18, 2013

NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen Tibial Baseplates are part of the NexGen systems of semi-constrained, non-…

FDA Devices Moderate Dec 18, 2013

NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplas…

FDA Devices Moderate Dec 18, 2013

Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobili…

FDA Devices Moderate Dec 18, 2013

NexGen Complete Knee Solution CR Articular Surface Provisional-Yellow 9mm Height Nonsterile Devices are used in total knee arthroplasty and indic…

FDA Devices Moderate Dec 18, 2013

NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm Height Nonsterile Devices are used in total knee arthroplasty and indi…

FDA Devices Moderate Dec 18, 2013

NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplas…

FDA Devices Moderate Dec 18, 2013

Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobilit…

FDA Devices Moderate Dec 18, 2013

NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green 9mm Height Nonsterile Devices are used in total knee arthroplasty an…

FDA Devices Moderate Dec 18, 2013

Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility…

FDA Devices Moderate Nov 27, 2013

Trinica Anterior Lumbar Plate (ALP) system, part 07.01058.001. Non Sterile, Rx only. The Trinica Anterior Lumbar Plate System is a temporary supplem…

FDA Devices Moderate Nov 20, 2013

VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys Heritage Hip System Revision Femoral Stems. Indicated for total hip arthro…

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.