PlainRecalls

Zimmer Biomet, Inc.

584 recalls on record · Latest: Dec 30, 2020

Zimmer Biomet, Inc. Recall Insight

Zimmer Biomet, Inc. appears on 584 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.696% 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 Jul 10, 2019 to Nov 13, 2019.

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 Nov 13, 2019

DIST LAT FEM LCK PLATE STERILE, Item Nos. 47235710106 47235710110 47235710114 47235710118 47235710122 47235710210 47235710214 47235710218 4…

FDA Devices Moderate Nov 13, 2019

Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009 47249318010 47249318011 47249318013 47249318014 47249318109 47249318110 4724…

FDA Devices Moderate Nov 13, 2019

Various Devices for Limb salvage arthroplasty, Item Nos. 00585000011 00585001201 00585001202 00585001301 00585001302 00585003038 00585003214 0…

FDA Devices Moderate Nov 13, 2019

PERIARTICULAR PLATES SHOULDER, PERI PROX LAT HUMERAL, Item Nos. 00234800104 00234800106 00234800108 00234800110 00234800112 00234800114 0023480…

FDA Devices Moderate Nov 13, 2019

NCB Straight Narrow Plate, various sizes, Item Nos. 0202267008 0202267010 0202267012 0202267014 0202267016 0202267018

FDA Devices Moderate Nov 13, 2019

FEMOROTIBIAL/FEMORAL NAIL, various sizes. Item Nos. 32855331111 32855331113 32855331115 32855331161 32855331163 32855331165

FDA Devices Moderate Nov 13, 2019

cable button for NCB¿ Polyaxial Locking Plate, 2.5 mm Hex Drive, Item No. 47223206001

FDA Devices Moderate Nov 13, 2019

CLS Brevius Stem Kinectiv, hip prosthesis, various sizes. Item Nos. 0100296050 0100296060 0100296070 0100296080 0100296090 0100296100 010029611…

FDA Devices Moderate Nov 13, 2019

CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 79 mm Item # 195758

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 65 mm Item # 195752

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Porous Plasma 91 mm Item # 195291

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 75 mm Item # 195251

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 59 mm Item # 195750

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 63 mm Item # 195245

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 75mm Item # 195275

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 87 mm Item # 195278

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 73 mm Item # 195250

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 83 mm Item # 195759

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 73 mm Item # 195756

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 91 mm Item # 195279

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 79 mm Item # 195252

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 67 mm Item # 195247

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 83 mm Item # 195277

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 69 mm Item # 195754

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 65 mm Item # 195246

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 63mm Item # 195269

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 67 mm Item # 195753

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 69 mm Item # 195248

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 75 mm Item # 195757

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 71mm Item # 195273

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 65mm Item # 195270

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 73mm Item # 195274

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 79 mm Item # 195276

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 63 mm Item # 195751

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 71 mm Item # 195249

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 71 mm Item # 195755

FDA Devices Moderate Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812

FDA Devices Moderate Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811

FDA Devices Moderate Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815

FDA Devices Moderate Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810

FDA Devices Moderate Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813

FDA Devices Moderate Aug 21, 2019

Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814

FDA Devices Moderate Jul 24, 2019

Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to provide proper irrigation du…

FDA Devices Moderate Jul 24, 2019

Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510

FDA Devices Moderate Jul 24, 2019

Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during th…

FDA Devices Moderate Jul 24, 2019

Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509

FDA Devices Moderate Jul 10, 2019

DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantati…

FDA Devices Moderate Jul 10, 2019

DVR Crosslock ePAK Depth Gauge, Model Number 212000003 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantatio…

FDA Devices Moderate Jul 10, 2019

K-Wire Trochar Tip, Model Number 212000008 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthope…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Zimmer Biomet, Inc. with FORD →

Data Sources

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