Ethicon, LLC

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

Ethicon, LLC 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 Ethicon, LLC

Date Product Reason Class
Aug 15, 2025 STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device, SFX S... Potential for barb non-engagement. Class II
Dec 20, 2024 PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H; Perma-hand Silk Sutur... Sutures may have an open seal on the primary packaging, due to a manufacturin... Class II
Dec 20, 2024 ETHIBOND EXCEL Polyester Suture, REF: 6664H, X425H, X872H, EH7491H. Not so... Sutures may have an open seal on the primary packaging, due to a manufacturin... Class II
Dec 20, 2024 PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLEN... Sutures may have an open seal on the primary packaging, due to a manufacturin... Class II
Aug 10, 2023 PDS II (polydioxanone) Suture, Product Numbers Z844G-50, D10065-05, D10085-05... Internal testing on returned product from this lot confirmed that some PDS" I... Class II
Aug 10, 2023 PDS Plus Antibacterial (polydioxanone) Suture, Product Numbers PDP072H40, PDP... Internal testing on returned product from this lot confirmed that some PDS" I... 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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