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Class 2 Device Recall Power Processor 3K and 3K High Speed Stockyards |
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Date Initiated by Firm |
July 28, 2021 |
Date Posted |
October 14, 2021 |
Recall Status1 |
Open3, Classified |
Recall Number |
Z-0117-2022 |
Recall Event ID |
88615 |
510(K)Number |
K110413
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Product Classification |
Radioassay, vitamin b12 - Product Code CDD
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Product |
Power Processor 3K, 3K High Speed Stockyards
Module Nameplate:
PP 3K Stockyard (Refrig) 9707 REF A88116 |
Code Information |
Catalog Number:
A88116 - 3K HS Refrigerated Stockyard
UDI: 15099590591960
Serial Numbers:
90HF1304006;
90HF1306009;
90HF1303005;
90HF1508005;
90HF1302005;
90HF1610005;
90HF1806001;
90HF1209005;
90HF1303007;
90HF1708006;
90HF1205001;
90HF1805002;
90HF1402005;
90HF1503001;
90HF1104002;
90HF1208004;
90HF1208005;
90HF1203001;
90HF1012004;
90HF1101002;
90HF1702003;
90HF1402004;
90HF1303008;
90HF1210001;
90HF1207001;
90HF1305007;
90HF1305004;
90HF1610001;
90HF1505002;
90HF1307005;
90HF1610002;
90HF1508003;
90HF1210002;
90HF1306001;
90HF1206002;
90HF1208002;
90HF1305008;
90HF1009002;
90HF1101001;
Catalog Number:
6915556 - Power Processor 3K Stockyard (Stockyard 3000/R Kit for PWR PROC)
Serial Numbers:
90AM0805001;
90AM0902009;
90AM0902005;
90AM0806003;
90AM0801003;
90AM0802002;
90AM0803001;
90AM0912002;
90AM1003002;
90AM0905010;
90AM0801004;
90AM06007008;
90AM060703;
90AM060704;
90AM0710002;
90AM0905007;
90AM0710008;
90AM0903002;
90AM0808002;
90AM0711004;
90AM0711005;
90AM0810001;
90AM0901002;
90AM0905006;
90AM0904004;
90AM0904005;
90AM0803002;
90AM0710004;
Amended - additional Products and Codes (12/15/2021):
B05520 - Stockyard, 5K HS, Refrigerated
Serial Numbers:
90HG1104002;
90HG1101001;
90HG1105002;
90HG1104001;
90HG1101003;
90HG1101002;
90HG1202004;
90HG1102005;
90HG1101004;
90HG1206002;
A88115 - 5K HS Refrig Stockyard
Serial Numbers:
90HG0911001
90HG0911003
90HG0911002
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Recalling Firm/ Manufacturer |
Beckman Coulter Inc. 250 S Kraemer Blvd Brea CA 92821-6232
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For Additional Information Contact |
Lindsey Whittaker 714-961-3614
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Manufacturer Reason for Recall |
Missing splash guard which may expose users to hazardous materials. .
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FDA Determined Cause 2 |
Process control |
Action |
During the week of 08/30/2021, the Recalling Firm sent an "URGENT MEDICAL DEVICE RECALL" Notification via its Field Action Notification process. On 09/16/2021, the Recalling Firm communicated a updated/revised "URGENT MEDICAL DEVICE RECALL" Notification letter which informed customer that, as a result of internal investigations, the Recalling Firm has discovered that the track-level splash guard has not been consistently provided to all customers. This guard is required for safe operation of the Power Processor system and could potentially cause user injuries if the splash guard is not in place.
Customer are being informed that a Recalling Firm Field Service representative will check their system for the splash guard. if the splash guard is not present, the Field Service representative will order and install it.
Customers are instructed to:
1. Continue to follow all safety warnings and system operation information provided in the Instructions for Use.
2. Share this information with their laboratory staff and to retain this notification as part of their laboratory Quality System documentation.
3. If customers have forwarded any of the affected products to another laboratory, provide a copy of this notification to them.
4. To confirm receipt of this Notification, customer are asked to respond within 10 days in one of the following ways:
-Electronically, if you received this communication via email.
-Manually, complete and return the enclosed Response Form.
Any questions, contact the Recalling Firm's Customer Support Center or their local representative via website http://www.beckmancoulter.com
Update 12/15/2021:
On 12/13/2021, the firm sent an "URGENT MEDICAL DEVICE RECALL" Letter informing of additional products being added to the original Recall initiated in 08/2021 for the missing splash guards. A Recalling Firm's Representative will check the systems and if a splash guard is not present, they will order and install it. In addition, the Recalling Firm is a |
Quantity in Commerce |
Total Units=271 units [258 units (3K and 3K HS); 13 units (5K added 12/15/2021)] |
Distribution |
U.S. Nationwide Distribution in the states of: CA, GA, IA, ID, IL, IN, LA, MA, MI, MS, NJ, NY, OH, OR, PA, SC, SD, TN, TX, WA, and WV
O.U.S.: Canada, China, Spain, France, United Kingdom, Israel, Italy, South Korea, Kuwait, Lebanon, Mexico, Malaysia, Netherlands, Portugal, Qatar, Saudi Arabia, Thailand, Turkey, and Taiwan. Additional O.U.S. added 12/15/2021 - South Africa |
Total Product Life Cycle |
TPLC Device Report
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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510(K) Database |
510(K)s with Product Code = CDD and Original Applicant = BECKMAN COULTER, INC.
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