Stryker GmbH
68 recalls on record · Latest: Jun 18, 2025
Stryker GmbH Recall Insight
Stryker GmbH appears on 68 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.067% 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 Jun 18, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.
On this page of 18 entries, severity tagging shows 0 critical, 18 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 8 of 18 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 (18). The date window on this page runs from May 2, 2018 to Jul 18, 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.
Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
Femoral Nail, A/R, R1500 T2 Femur ¿12x300 mm, Product Number 18281230S
Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
Femoral Nail, LEFT T2 GTN ¿14x300 mm, Product Number 18501430S
Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
Femoral Nail, LEFT T2 GTN ¿10x360 mm, Product Number 18501036S
Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
Femoral Nail, A/R, R1500 T2 Femur ¿12x380 mm, Product Number 18281238S
Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity corr…
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Data Sources
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.