Malosa Core SMILE Pack 2-Beaver-Visitec- A Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK967
FDA Recall Z-0410-2022 · Posted None
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Recalling FirmBeaver Visitec International, Inc.
Recall StatusOpen, Classified
Product CodePZG
Date Initiated2021-11-17
Product Quantity1170 units
Reason for Recall
Kit packaging may have small holes compromising product sterility
Firm Action
Beaver Visitec issued Urgent Medical Device Recall notification dated 11/17/21 to the first level consignee. Letter states reason for recall, health risk and action to take:
PLEASE perform the following actions:
1. Immediately examine your inventory and quarantine product from these lots that are subject to recall.
If you have further distributed this product, please notify your customers by initiating a sub-recall. Consider all potential users of this product in your user supply chain. You are encouraged
to use a copy of this recall notification letter when contacting your customers.
2. Complete the enclosed Business Reply Form (BRF) and indicate whether you have affected product to return.
3. Please enter the following information on the enclosed BRF: part number(s), lot number(s) and quantity(ies) of device(s) that are being returned.
4. Return the completed BRF to BVI by one of these methods:
" Fax to 866-912-8416
" Email the attached to [email protected]
5. Return your product to STERICYCLE using the enclosed UPS pre-paid return label:
Stericycle
2670 Executive Drive, Suite A
Indianapolis, IN 46241
Attn: Event 3570
If you have questions regarding the return procedure, please contact Stericycle Inc. at 866-625-5325 (Mon.-Fri. 8:00 am - 5:00 pm Eastern Time).
Root Cause
Packaging change control
Distribution Pattern
CA, CO, LA, MA, MD, ND, PA, TN, UT
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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