FDA recall record

DePuy Mitek, Inc., a Johnson & Johnson Co 1113 Gravity Tube Set Pk/24 -SH Product Usage: The recall — FDA Z-0695-2018

Leakage of FMS gravity tub sets (281113) at the bulb and tube connection

Class IIclassification
Z-0695-2018official record ID
Mar 7, 2018report date

Recall record at a glance

Official recordZ-0695-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDePuy Mitek, Inc., a Johnson & Johnson Co.
Report dateMar 7, 2018
Recall initiation dateAug 31, 2017
Quantity15,678
LocationRaynham, MA, United States

Official product description

1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Gravity Tube Set is intended to deliver irrigation fluid from irrigation containers to the operative site during arthroscopic procedures.

Why the product was recalled

Leakage of FMS gravity tub sets (281113) at the bulb and tube connection

Distribution information

US Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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