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 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 Feb 7, 2018 to Mar 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 Mar 7, 2018

979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.

FDA Devices Moderate Mar 7, 2018

Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item No. 00585001202); c. S…

FDA Devices Moderate Mar 7, 2018

Ziptight Ankle Syndesmosis Fixation Device, Titanium Implant Titanium Implant for surgical repairs of soft tissue.

FDA Devices Moderate Mar 7, 2018

The 2nd Assist Knee Positioner

FDA Devices Moderate Mar 7, 2018

Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled as follows: a. VERSYS 6 INCH BEADED FC 19X160MM STD BODY STD NECK (Item No. 008943019…

FDA Devices Moderate Mar 7, 2018

Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt. orthopedic instrument

FDA Devices Moderate Feb 28, 2018

ROSA Brain 3.0 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and orientation of instrument holder…

FDA Devices Moderate Feb 28, 2018

Vanguard Complete Knee System, Vanguard CR Lipped Tibial Bearing 10x71/75, Item Number: 183540 Product Usage: For use in total knee arthroplasty

FDA Devices Moderate Feb 28, 2018

ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and orientation of instrument hold…

FDA Devices Moderate Feb 28, 2018

Vanguard Complete Knee System, Vanguard CR Tibial Bearing 12x71/75, Item Number: 183442 Product Usage: For use in total knee arthroplasty

FDA Devices Moderate Feb 21, 2018

G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissu…

FDA Devices Moderate Feb 21, 2018

AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Arthroplasty.

FDA Devices Moderate Feb 21, 2018

Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implantation of PP…

FDA Devices Moderate Feb 21, 2018

AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For use in Total Knee Arthroplasty.

FDA Devices Moderate Feb 21, 2018

BlockAid Cut Resistant Surgical Glove Liners, combine stainless steel and synthetic fibers woven together to form a cut resistant glove material. Blo…

FDA Devices Moderate Feb 14, 2018

M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only, Item Number 00-2255-025-00 Product Usage: …

FDA Devices Moderate Feb 14, 2018

M/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 mm Diameter 70 cm Length Single Use Only, Item Number 00-2255-026-00 Product Usag…

FDA Devices Moderate Feb 14, 2018

Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length, Item Number 47-2255-008-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are us…

FDA Devices Moderate Feb 14, 2018

Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length, Item Number 47-2490-098-00 Product Usage: The Ball Tip and Tear D…

FDA Devices Moderate Feb 14, 2018

Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 70 cm length, Item Number 47-2490-098-01 Product Usage: The Ball Tip and Tear D…

FDA Devices Moderate Feb 14, 2018

DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, 125 DEG 11MM X 180MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 11MM X 360MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 440MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 11MM X 440MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 340MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 400MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 320MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 400MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 340MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 320MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, 130 DEG 9MM X 180MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 13MM X 440MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 360MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 9MM X 380MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 9MM X 440MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, 130 DEG 11MM X 180MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 11MM X 460MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 260MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 9MM X 300MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 380MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 260MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 13MM X 460MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 130 DEG 11MM X 460MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 125 DEG 9MM X 400MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 11MM X 440MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 9MM X 380MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, RH 130 DEG 11MM X 280MM

FDA Devices Moderate Feb 7, 2018

Affixus Hip Fracture Nail, LH 125 DEG 9MM X 340MM

Nearby Manufacturers

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Compare Zimmer Biomet, Inc. with MEDLINE INDUSTRIES, LP - Northfield →

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.