Medical Device Recall: Z-1794-2020

FDA Recalls dataset · Firm: Alcon Research LLC · Status: Terminated

Recall Action Class: N/A Date Initiated: 2018-07-25 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-1794-2020.

Recall Res Number
Z-1794-2020
Recalling Firm / Manufacturer
FEI Number
1610287
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2018-07-25
Date Posted
N/A
Date Terminated
2020-04-24
Product Code
HQC
Event Number
85198
Product Quantity
102 packs
Product Description Alcon Constellation Vision System 20 GA TOTALPLUS Combined Procedure Pak, Product #8065751079, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.

Reason for Recall There was a potential that a 25-gauge infusion cannula may be included within the procedure pak instead of a 20-gauge infusion cannula.

Action Details The firm issued undated letters to the foreign consignees on 7/25/2018 advising them of the issue and to return affected product.

Distribution Pattern There was no domestic distribution. Foreign distribution was made to Germany, Iraq, Israel, Italy, and Moldova.

Code Information / Serial Numbers Lot #2128524H

Related Establishments / Registrations

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