FDA recall record

Alcon Research SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon recall — FDA Z-1370-2024

Medline Bulb irrigation syringes recalled due to potential for packaging sterile barrier to be breached, and these syringes were packed inside surgical…

Class IIclassification
Z-1370-2024official record ID
Apr 3, 2024report date

Recall record at a glance

Official recordZ-1370-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAlcon Research, LLC
Report dateApr 3, 2024
Recall initiation dateFeb 21, 2024
Quantity886
LocationHouston, TX, United States

Official product description

SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon Custom-Pak Surgical Procedure Packs, Products: 18018-06, 3865-44, 5675-76, 13554-11, 18018-06, 15190-16 , 15190-16, 15190-16, 15190-16, 15190-16, 13554-11, 5918-39, 15190-16, 15190-16, 9208-66, 9208-66, 5675-76, 5918-39, 9208-66, 15190-16, 9065-25, 5918-39, 16066-15, 16066-15

Why the product was recalled

Medline Bulb irrigation syringes recalled due to potential for packaging sterile barrier to be breached, and these syringes were packed inside surgical procedure packs that were subsequently terminally sterilized, so after the packs are opened, syringes should be discarded at surgical case end, and not reshelved, because the use of non-sterile bulb irrigation syringes may increase infection risk.

Distribution information

US Nationwide distribution in the states of OH, WV.

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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Class IIFDA: OngoingAlcon Research LLC