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Class 2 Device Recall Medline Convenience kits |
![see related information](../images/related-info.gif) |
Date Initiated by Firm |
June 06, 2022 |
Create Date |
July 27, 2022 |
Recall Status1 |
Open3, Classified |
Recall Number |
Z-1475-2022 |
Recall Event ID |
90516 |
Product Classification |
Skin prep tray - Product Code OJU
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Product |
Medline Convenience kits labeled as: a. WET SKIN PREP TRAY, b. SKIN PREP TRAY W/CHG Model/Catalog Number: Model numbers: a. DYNDP1127A, b. DYNDP1131
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Code Information |
Lot Code: a. Model number DYNDP1127A, Lot Numbers: 22ABG455, 21FBU537, 21IBF632, 21JBY751, 21LBB154, b. Model number DYNDP1131, Lot Numbers: 22DBT130, 22DBK391, 22ABC822, 22OBE201, 21IBR746, 21JBL238, 21KBU021. |
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 |
1880 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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