PlainRecalls
FDA Devices Moderate Class II Terminated

MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

Reported: February 17, 2021 Initiated: January 4, 2021 #Z-1068-2021

Product Description

MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

Reason for Recall

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

Details

Recalling Firm
Aomori Olympus Co., Ltd.
Units Affected
7,400,000 (globally); 260,395 (US)
Distribution
US Nationwide distribution.
Location
Kuroishi, N/A

Frequently Asked Questions

What product was recalled?
MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.. Recalled by Aomori Olympus Co., Ltd.. Units affected: 7,400,000 (globally); 260,395 (US).
Why was this product recalled?
Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 17, 2021. Severity: Moderate. Recall number: Z-1068-2021.