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 14, 2012 to Dec 26, 2012.

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 Dec 26, 2012

Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable Regular Humerals STERILE Rx, Tivanium QTY/PKG:1 Product Usage: The ulnar…

FDA Devices Moderate Dec 26, 2012

Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size G Left; Size G Right This device is used with the Persona…

FDA Devices Moderate Dec 26, 2012

Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size E Left; Size E Right This device is used with the Persona…

FDA Devices Moderate Dec 26, 2012

Persona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivanium Sterile TIBIA SIZE G, LEFT TIBIA SIZE G RIGHT This de…

FDA Devices Moderate Dec 26, 2012

Persona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size H Left; Size H Right This device is used with the Persona…

FDA Devices Moderate Dec 26, 2012

Persona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivanium Sterile This device is indicated for patients with se…

FDA Devices Moderate Dec 5, 2012

NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ system is a semiconstrained, nonlinked condylar knee prostheses.…

FDA Devices Moderate Nov 28, 2012

00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Femoral Head Provisional 40mm +0 00789504003 VerSys Femoral Head Provision…

FDA Devices Moderate Nov 28, 2012

00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202 MIS 12/14 Slotted Femoral Head Provisional +0X32 00780303203 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780304003 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS 12/14 Slotted Femoral Head Provisional +0X22 00780302203 MIS 12/14 Slo…

FDA Devices Moderate Nov 28, 2012

Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplast…

FDA Devices Moderate Nov 28, 2012

00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780303603 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

The Trilogy Acetabular System Shell with Cluster Holes Porous 56 mm O.D. Sterile The Trilogy Acetabular System is indicated for either cement…

FDA Devices Moderate Nov 28, 2012

. 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys Femoral Head Provisional 28mm +0 00789502803 VerSys Femoral Head Provisi…

FDA Devices Moderate Nov 28, 2012

00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802 MIS 12/14 Slotted Femoral Head Provisional +0X28 00780302803 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

Multipolar¿ Bipolar Cup Liner 22 mm LD.; Item 00-5001-040-22 Product Usage: The liner snaps into the Multipolar¿ Bipolar Cup and serves as the …

FDA Devices Moderate Nov 28, 2012

00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602 MIS 12/14 Slotted Femoral Head Provisional +0X26 00780302603 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys Femoral Head Provisional 32mm +0 00789503203 VerSys Femoral Head Provision…

FDA Devices Moderate Nov 28, 2012

Product 100789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys Femoral Head Provisional 22mm +3.5 00789502220 VerSys Femoral Head …

FDA Devices Moderate Nov 28, 2012

00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys Femoral Head Provisional 26mm +0 00789502603 VerSys Femoral Head Provision…

FDA Devices Moderate Nov 28, 2012

. 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys Femoral Head Provisional 36mm +0 00789503603 VerSys Femoral Head Provisi…

FDA Devices Moderate Nov 21, 2012

ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended to be used by qualified medical professionals to temporarily occlude blood…

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw

FDA Devices Moderate Nov 14, 2012

NCB¿ screw ¿ 4.0 self-tapping

FDA Devices Moderate Nov 14, 2012

DTO" Implant

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Fracture Humeral stem

FDA Devices Moderate Nov 14, 2012

Alloclassic SL Shaft

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Biolox¿ Option Ceramic Femoral Head System Rx, sterile

FDA Devices Moderate Nov 14, 2012

zimmer Anatomical Shoulder Glenoid S, cemented, sterile; REF 01.04214.340 PE Keeled Glenoid S, cemented, sterile; REF 01.04214.345, Glenoid M, ce…

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Inverse Humeral Cup

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Inverse/Reverse Glenoid Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Revision + set screw

FDA Devices Moderate Nov 14, 2012

MS-30¿ Stem

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Humeral stem

FDA Devices Moderate Nov 14, 2012

MS-30¿ Distal centralizer, cemented, sterile, Rx

FDA Devices Moderate Nov 14, 2012

CLS Stem

FDA Devices Moderate Nov 14, 2012

Original M.E. Mueller" Low Profile Cup Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Humeral Head

FDA Devices Moderate Nov 14, 2012

NCB¿ cancellous screw

FDA Devices Moderate Nov 14, 2012

Kopf Adapter S Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Fitmore" Hip Stem

FDA Devices Moderate Nov 14, 2012

Dynesys¿ HA Pedicle + set screw

FDA Devices Moderate Nov 14, 2012

NCB¿-PH Plate

FDA Devices Moderate Nov 14, 2012

Metasul¿ Durom¿ Femoral component Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Set screw M6

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Universal spacer 6-45

FDA Devices Moderate Nov 14, 2012

NCB¿-PT lateral proximal 3 hole tibial plate

FDA Devices Moderate Nov 14, 2012

Dynesys¿ L.I.S. Stabilizing cord Rx, Sterile

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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.