PlainRecalls

Zimmer GmbH

64 recalls on record · Latest: Sep 18, 2024

Zimmer GmbH Recall Insight

Zimmer GmbH appears on 64 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.076% 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 Sep 18, 2024, 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 May 29, 2019 to Sep 18, 2024.

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 Sep 18, 2024

Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and acetabular…

FDA Devices Moderate Jun 9, 2021

Zimmer Natural Nail -ZNN Cephalomedullary Short Nail 11.5 mm X 21.5 cm 125 CCD Left Ti-6Al-4V Alloy- intended for temporary fracture fixation and sta…

FDA Devices Moderate Jun 9, 2021

Zimmer Natural Nail- ZNN Cephalomedullary Short Nail 11.5 mm X 21.5 cm 130 CCD Left Ti-6Al-4V Alloy-is intended for temporary fracture fixation and s…

FDA Devices Moderate May 29, 2019

V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, contra-angle, Item Number 502015637

FDA Devices Moderate May 29, 2019

Drill, contra-angle, 1.5x85mm, Item Number ST502015706

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3x90mm, AO, Item Number ST502015631

FDA Devices Moderate May 29, 2019

CBS micro, countersink, cannulated, round-shaft, Item Number 503004341

FDA Devices Moderate May 29, 2019

Drill, 15mm stop, 1x83mm, Stryker, Item Number 502015114

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.5x95mm, AO, Item Number 502015621

FDA Devices Moderate May 29, 2019

Drill for 3.5mm screw, 2.5x120mm, AO, Item Number ST502015216

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.8x150mm, AO, Item Number 502015629

FDA Devices Moderate May 29, 2019

V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, AO, Item Number 502015638

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3x90mm, round shaft, Item Number 502015630

FDA Devices Moderate May 29, 2019

CBS 4.0 countersink, cannulated, 15mm stop, AO, Item Number 503004352

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.8x120mm, AO, Item Number ST502015628

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x120mm, AO, Item Number ST502015402

FDA Devices Moderate May 29, 2019

Drill for 2.7mm screw, 2x120mm, AO, Item Number 502015212

FDA Devices Moderate May 29, 2019

Drill, 26mm stop, 1.4x94mm, Stryker, Item Number 502015120

FDA Devices Moderate May 29, 2019

CBS 7.5 tap, cannulated, AO, Item Number 503002041

FDA Devices Moderate May 29, 2019

Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number ST502015207

FDA Devices Moderate May 29, 2019

Drill for 3.5mm screw, 2.5x120mm, AO, Item Number 502015216

FDA Devices Moderate May 29, 2019

Drill, 26mm stop, 1.4x94mm, stryker, Item Number 502015145

FDA Devices Moderate May 29, 2019

V-TEK", Micro-countersink, AO, Item Number 28.66.113

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, round shaft, Item Number 502015619

FDA Devices Moderate May 29, 2019

CBS high, countersink, cannulated, round-shaft, Item Number 503004342

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.8x120mm, AO, Item Number 502015628

FDA Devices Moderate May 29, 2019

Drill, 2.5x135mm, AO, Item Number 502015142

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x90mm, round shaft, Item Number ST502015640

FDA Devices Moderate May 29, 2019

CBS 4.5 countersink, cannulated, 18mm stop, round-shaft, Item Number 503004351

FDA Devices Moderate May 29, 2019

Drill, 3.2x145mm, AO, Item Number ST502015650

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, AO, Item Number 502015623

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3.5x90mm, round shaft, Item Number ST502015635

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.5x95mm, AO, Item Number ST502015621

FDA Devices Moderate May 29, 2019

Drill, contra-angle, 1.5x85mm, Item Number 502015706

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3x90mm, AO, Item Number 502015631

FDA Devices Moderate May 29, 2019

CBS micro, countersink, cannulated, AO, Item Number 503004541

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3.5x90mm, round shaft, Item Number 502015635

FDA Devices Moderate May 29, 2019

V-TEK", micro-countersink, round shaft, Item Number 28.66.112

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, round shaft, Item Number ST502015619

FDA Devices Moderate May 29, 2019

Drill Sys2.7, 2x103mm, AO, Item Number 502015107

FDA Devices Moderate May 29, 2019

Osteofresh arthrodesis drill, 2x70mm, center tip, AO, 10mm stop, Item Number 502015213

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x90mm, round shaft, Item Number 502015640

FDA Devices Moderate May 29, 2019

Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106

FDA Devices Moderate May 29, 2019

Drill, 2.5x94mm, Stryker, Item Number 502015136

FDA Devices Moderate May 29, 2019

V-TEK", standard-countersink, cannulated, AO, Item Number 28.66.111

FDA Devices Moderate May 29, 2019

Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131

FDA Devices Moderate May 29, 2019

Drill, 2.5x87mm, AO, Item Number 502015137

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, AO, Item Number ST502015623

FDA Devices Moderate May 29, 2019

Drill, 15mm stop, 1x76mm, AO , Item Number 502015115

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x150mm, AO, Item Number ST502015403

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Zimmer GmbH 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