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 47 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 Sep 18, 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

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 Nov 13, 2019

Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519 47235800603 47235800605 4723…

FDA Devices Moderate Nov 13, 2019

TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 00450001200 00450001300 00450001400 00450001500 00450001600 00450002100 00450002200 00450…

FDA Devices Moderate Nov 13, 2019

Metasul Taper Liner, various sizes, Item Nos. 00877000528 00877000628 00877000732 00877000832 00877000936 00877001036 00877001140 00877001240 …

FDA Devices Moderate Nov 13, 2019

Various Surgical Instruments: Screws and Reamers, Item Nos. 00579104100 00579104200 00579104300 00579104400 00579105400 00597909526 00597909529…

FDA Devices Moderate Nov 13, 2019

Periarticulare Plates - Elbow, Humeral and Ulna Plates, Item Nos. 00234800504 00234800506 00234800508 00234800510 00234800512 00234800514 00234…

FDA Devices Moderate Nov 13, 2019

Sidus Stem-Free Shoulder Humeral Head, Item Nos. 0104555380 0104555400 0104555420 0104555440 0104555460 0104555480 0104555485 0104555500 0104…

FDA Devices Moderate Nov 13, 2019

PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos. 00234801303 00234801304 00234801306 00234801308 00234801310 00234801312 00234801403 …

FDA Devices Moderate Nov 13, 2019

Trabecular Metal Reverse Shoulder System, Item Nos. 00434210613 00430900103 00434210613 00434210813 00434210817 00434210913 00434211013 004342…

FDA Devices Moderate Nov 13, 2019

Fitmore Hip Stem, hip prosthesis, various sizes, Item Nos. 0100551102 0100551103 0100551104 0100551105 0100551106 0100551107 0100551108 010055…

FDA Devices Moderate Nov 13, 2019

Coorad Morrey Total Elbow, Item Nos. 32810502501 32810502701 32810502900 32810503000 32810600012 32810600013 32855510796 32855510797 32855510…

FDA Devices Moderate Nov 13, 2019

Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 00151505040 00151505240 00151505444 001515056…

FDA Devices Moderate Nov 13, 2019

Various Custom Devices, Item Nos. 32855090246 32855090252 32855090256 32855090265 32855090266 32855090270 32855090287 32855090290 32855090291…

FDA Devices Moderate Nov 13, 2019

NCB Proximal Lateral Tibia, "NCB-PT LAX PROX 3H TIBIA", Various Sizes, Item Nos. 0202261205 0202261207 0202261209 0202261213 0202261305 02022613…

FDA Devices Moderate Nov 13, 2019

SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 47235802108 47235802203 47235802204 …

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 Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 87 mm Item # 195254

FDA Devices Moderate Sep 18, 2019

XP-XP Tibial Tray - Interlok 87 mm Item # 195760

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 67mm Item # 195271

FDA Devices Moderate Sep 18, 2019

XP-CR Tibial Tray - Interlok 69mm Item # 195272

FDA Devices Moderate Sep 18, 2019

Vanguard XP Tibial Tray 83 mm Item # 195253

Nearby Manufacturers

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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.