Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1453-2025Class II

Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE...

MEDLINE INDUSTRIES, LP - Northfield / initiated 2025-02-11 / Open, Classified

MEDLINE INDUSTRIES, LP - Northfield began a recall of Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number 613034702 on . FDA classified it as Class II and gives the reason as "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health". As of , the recall status on record is Open, Classified.

Recall record

Recall number
Z-1453-2025
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number 613034702
Product code
HRX Arthroscope
Reason for recall
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
FDA root cause
Under Investigation by firm
Action
Medline Industries LP issued a recall notice to its consignees on 02/11/2025 via letter delivered via USPS and email. The notice explained the issue, provided a link to for information pertaining to the risk involved https://www.fda.gov/medical-devices/safety-communications/update-evaluating-plastic-syringes-made-china-potential-device-failures-fda-safety-communication) and request the syringes within the convenience be discarded, except for circumstances where no alternative syringes are readily available. If these syringes must be used, closely monitor for leaks, breakage, and any other problems, and report any quality issues to Medline and the FDA. Distributors were directed to notify their customers. This is an expansion of RES 94583
Quantity in commerce
90 units
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Product codes and lots
1) Pack Number 613034700: UDI/DI 10850009724004 (each) 40850009724005 (case), Lot Number 613034700; 2) Pack Number 613034702: UDI/DI 10850009724066 (each) 40850009724067 (case), Lot Number 613034702

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1453-2025
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1435-2025Class IIOngoingVoluntary: Firm initiated
Z-1436-2025Class IIOngoingVoluntary: Firm initiated
Z-1437-2025Class IIOngoingVoluntary: Firm initiated
Z-1438-2025Class IIOngoingVoluntary: Firm initiated
Z-1439-2025Class IIOngoingVoluntary: Firm initiated
Z-1440-2025Class IIOngoingVoluntary: Firm initiated
Z-1441-2025Class IIOngoingVoluntary: Firm initiated
Z-1442-2025Class IIOngoingVoluntary: Firm initiated
Z-1443-2025Class IIOngoingVoluntary: Firm initiated
Z-1444-2025Class IIOngoingVoluntary: Firm initiated
Z-1445-2025Class IIOngoingVoluntary: Firm initiated
Z-1446-2025Class IIOngoingVoluntary: Firm initiated
Z-1447-2025Class IIOngoingVoluntary: Firm initiated
Z-1448-2025Class IIOngoingVoluntary: Firm initiated
Z-1449-2025Class IIOngoingVoluntary: Firm initiated
Z-1450-2025Class IIOngoingVoluntary: Firm initiated
Z-1451-2025Class IIOngoingVoluntary: Firm initiated
Z-1452-2025Class IIOngoingVoluntary: Firm initiated
Z-1453-2025Class IIOngoingVoluntary: Firm initiated