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Class 2 Device Recall Medline convenience kits |
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Date Initiated by Firm |
June 06, 2022 |
Create Date |
July 27, 2022 |
Recall Status1 |
Open3, Classified |
Recall Number |
Z-1471-2022 |
Recall Event ID |
90516 |
Product Classification |
Central venous catheter tray - Product Code OFF
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Product |
Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot codes: 19UBB149, b. KIT LB SHUNT, Model NumberDYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567 Model/Catalog Number: a. Model Number DYNJ36725B, b. Model Number DYNJ905860A
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Code Information |
Lot Code: a. Model Number DYNJ36725B, Lot codes: 19UBB149, b. Model Number DYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567
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Recalling Firm/ Manufacturer |
MEDLINE INDUSTRIES, LP - SPT 1170 S Northpoint Blvd Waukegan IL 60085-6757
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For Additional Information Contact |
Kassandra Cotner 866-775-6072
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Manufacturer Reason for Recall |
Kits contain leaking bottles of isopropyl alcohol
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FDA Determined Cause 2 |
Under Investigation by firm |
Action |
The firm's consignees were notified by US mail on 06/06/2022 and instructed to destroy any affected kits on hand in accordance with their local and state regulations. |
Quantity in Commerce |
288 units |
Distribution |
US Nationwide distribution. |
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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