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Clover Discectomy Set

KOROS U.S.A., INC. · Model 7332-70 · UDI-DI 10840199543707

GAD Prescription

510(k) clearances

1,660

Adverse events (4 deaths)

Recalls

667

Facilities

Description

Clover Discectomy Set Consists of the Following: 1 x 7391-23, 1 x 7391-28, 1 x 7391-30, 1 x 7391-34, 1 x 7391-36, 1 x 7391-38, 1 x 7391-44, 1 x 7391-32, 1 x 7391-42, 1 x 7391-86, 1 x 7391-87, 1 x 7391-88, 1 x 7391-89, 1 x 7391-92, 1 x 7391-94, 1 x 7391-96, 1 x 7392-01, 1 x 7392-04, 1 x 7392-05, 1 x 7392-06, 1 x 7346-30, 1 x 7449-12 & 1 x 7332-80

Recalls

Date	Firm	Reason
2026-06-05	Integra LifeSciences Corp. (NeuroSciences)	The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110
2025-04-09	MEDLINE INDUSTRIES, LP - Northfield	Three is the potential for the retractors to puncture through the sterile packaging.
2024-12-03	Sklar Instruments	Reports of various packaging issues that may result in a breach of the sterile barrier.
2024-05-17	SEASPINE ORTHOPEDICS CORPORATION	Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure
2024-05-17	SEASPINE ORTHOPEDICS CORPORATION	Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure
2024-02-23	MEDLINE INDUSTRIES, LP - Northfield	Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
2023-12-21	Medagent Inc	Holding arm could move (twist) uncontrollably in the front area. This could lead to a serious deterioration of patient's safety if the movement is transferred to the spatula, which
2023-05-25	TELEFLEX LLC	There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
2023-05-25	TELEFLEX LLC	There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
2022-12-08	Medtronic Navigation, Inc.	Defect in sterile pouch seal, incomplete seal, of lighted Retractors, increases the risk of contamination, which can lead to post-operative infection.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.