PlainRecalls

Zimmer Biomet, Inc.

Compiled from official public sources by the editorial team.

875 recalls on record · Latest: Dec 30, 2020

Zimmer Biomet, Inc. Recall Insight

Zimmer Biomet, Inc. appears on 875 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.860% 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 Dec 30, 2020, 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 48 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 Dec 6, 2017 to Feb 7, 2018.

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 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 na…

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 p…

FDA Devices Moderate Dec 6, 2017

ROSA Surgical Device 2.5.8

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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.