MICROLINE SURGICAL, INC.
6 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (6)
Registered facilities (1)
- Microline Surgical, Inc FEI 1000137656 · MA
Recalls & enforcement
- Class IIOngoing2024-11-05A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.
- Class IITerminated2019-03-22The shears exhibited a high rate of complete or intermittent failure to actuate. As a result, they do not perform their intended function in surgical procedures.
- Class IITerminated2017-11-01Certain lots of disposable laparoscopic instrument tips may potentially have a compromised sterile barrier.
- Class IITerminated2017-07-13The heat-shrink insulation tube may split during autoclave sterilization/re-sterilization. If a split occurs, the heat-shrink could fall off during a surgical procedure and if cautery is needed, there is a potential for burn due to insulation failure.
- Class IITerminated2014-05-12Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw
- Class IITerminated2014-04-14Grasper jaw may break when force is applied to the jaw
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “MICROLINE SURGICAL, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9006317-microline-surgical-inc/
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