Water Filter MAJ-2318. This MAJ-2318 water filter has been designed to be used with Olympus endoscope reprocessor for prevent contamination of the rinse water. The MAJ-2318 water filter is compatible with OER-ELITE and OER-MINI.
FDA Recall Z-1009-2024 · Posted 2024-02-07
Advertisement
Recalling FirmOlympus Corporation of the Americas
Recall StatusOpen, Classified
Product CodeFEB
Date Initiated2024-01-16
Product Quantity877 MAJ-2318, 119 OER-Elite, 3 OER-MINI
Reason for Recall
Water filter may have been assembled incorrectly, resulting in unfiltered tap water being used for reprocessing. This may expose a patient to a potentially contaminated device, presenting a risk of infection or sepsis.
Firm Action
On January 16, 2024, the firm notified customers of the issue via URGENT MEDICAL DEVICE FIELD CORRECTIVE ACTION letters.
Customers were instructed to immediately assess all MAJ-2318 at their facility to check the model and lot number. Customers were given detailed instructions on how to identify affected product, including for MAJ-2318 installed in the OER machine.
Please contact your Olympus customer service representative at 1-800-848-9024, option 2 to obtain a Return Material Authorization to return any affected product.
Customers who have further distributed product should notify downstream accounts at once.
If you require assistance with identifying affected product, please contact the Olympus Technical Assistance Center at 1- 800-848-9024, option 1.
If you have questions about this recall, please contact the recalling firm at (647) 999-3203 or by e-mail at [email protected].
Root Cause
Process control
Distribution Pattern
Domestic US distribution nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement