Microline Surgical, Inc.
Microline Surgical, Inc. has 5 FDA enforcement events on this register (7 product records) between 2014 and 2024: 5 device; the busiest year was 2017 with 2.
0% of its events are Class I; the most common class is Class II (5). 1 event is listed as ongoing; the recalling firm's address is in MA.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 5 Nov 2024 | Microscissor Tip (Disposable); Microline Catalog #: 3122. | Device | Class II | 1 | Ongoing |
| 22 Mar 2019 | TLS2 Thermal Ligating Shears, Catalog Number 132-131D | Device | Class II | 1 | Terminated |
| 1 Nov 2017 | ReNew Dolphin Nose Disposable Dissector Tip, Catalog Number: 3312, UDI: 00811099011989 The ReNew single patient use disposable tips are to be used with the ReNew Laparoscopic Hand Pieces and they are indicated for cutting, grasping, dissecting and coagulation of tissue in endoscopic and laparoscopic surgical… | Device | Class II | 2 | Terminated |
| 13 Jul 2017 | The ReNew Reusable Grasper and Dissector Tips are to be used with the ReNew Laparoscopic Handpieces and they are indicated for cutting, grasping, dissecting, and coagulation of tissue in endoscopic and laparoscopic surgical procedures. | Device | Class II | 1 | Terminated |
| 12 May 2014 | Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221 | Device | Class II | 2 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Microline Surgical, Inc. had?
5 enforcement events (7 product records) on this register, 2014–2024: 5 device.
Are any Microline Surgical, Inc. recalls ongoing?
1 event is listed as ongoing in the current openFDA export.
What class are Microline Surgical, Inc. recalls?
5 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.