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Stryker Craniomaxillofacial Division

Complete recall history across all FDA and CPSC categories — 6 total recalls

Stryker Craniomaxillofacial Division appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (6)

FDA medical device enforcement actions by Stryker Craniomaxillofacial Division

Date Product Reason Class
Sep 17, 2015 Disposable Paper Filter for Sterilization Containers Paper, Medical Access... Stryker has become aware that the inhomogeneity of the filter paper might pot... Class II
Dec 17, 2014 MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB) R... Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained arti... Class II
Dec 17, 2014 MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot... Potential for implant damage, implant cracking off/breaking intra-operatively. Class II
Dec 17, 2014 MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implan... Potential for implant deformation, implant mechanical stability too low, loss... Class II
Dec 17, 2014 MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block, ... Potential for implant deformation, implant mechanical stability too low, loss... Class II
Jul 30, 2013 Stryker Part Numbers 79-43903 (3cc), 79-43905 (5cc), 79-43910 (10 cc), 79-439... Stryker received reports of the desiccant bag in the kit leaking silica gel g... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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