Gyrus Acmi, Inc.
11 recalls on record · Latest: Apr 24, 2019
Gyrus Acmi, Inc. Recall Insight
According to PlainRecalls' manufacturer ranking (distinct recall events, same sort as /rankings), Gyrus Acmi, Inc. sits #1,344 of 14,182 (1,344th among 14,182 firms) with 11 federal notices, about 0.011% of the 104,158-record FDA/CPSC/NHTSA archive. Rank counts issuance frequency, not danger or fault; large diversified firms accumulate more records by scale alone. 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 Apr 24, 2019, which is the anchor point for assessing whether enforcement is currently active or historical.
On this page of 11 entries, severity tagging shows 0 critical, 11 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 11 of 11 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 (11). The date window on this page runs from Apr 18, 2018 to Apr 24, 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.
Diego Elite Turbinate Blades:Bipolar Blade, 2mm straight, standard, type A Part No BB2000SA
Diego Elite Turbinate Blades Bipolar Blade, 4mm curved, Product Number: BB4040XC
Diego Elite Turbinate Blades Bipolar Blade, 4mm curved, Product Number: BB4040XS
Diego Elite Blades Monopolar, 4mm Straight, TIA Product Code:MB4000SS
Diego Elite Turbinate Blades Bipolar Blade, 4mm straight, Part Number: BB4000SS
Diego Elite Turbinate Blades Bipolar Blade, 4mm curved, Product Number:BB4040SS
Diego Elite Turbinate Blades Bipolar Blade, 4mm curved, Product Number: BB4040SC
Diego Elite Malleable, 4mm Standard Monopolar Blades Product Code:MM4000SS
Diego Elite Turbinate Blades Bipolar Blade, 4mm straight, Part No: BB4000SC
Olympus Diego Elite Console MDCONS 100
Gyrus ACMI Round Cutting Burrs - to be used with the Diego Elite system
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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 August 2026.