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Class 2 Device Recall DYNAREX |
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Date Initiated by Firm |
May 25, 2022 |
Date Posted |
August 26, 2022 |
Recall Status1 |
Open3, Classified |
Recall Number |
Z-1622-2022 |
Recall Event ID |
90336 |
Product Classification |
Pad, alcohol, device disinfectant - Product Code LKB
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Product |
Dynarex¿ PAD, NAIL POLISH REMOVER (100/BX 10BX/CS) DYNREX Catalog # 1501 |
Code Information |
GTIN: Not Available
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Recalling Firm/ Manufacturer |
Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233
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For Additional Information Contact |
Ms. Ruby Upadhyaya 804-553-2281
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Manufacturer Reason for Recall |
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
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FDA Determined Cause 2 |
Environmental control |
Action |
Mckesson Letter Notifcations issued via USP by or by email if available by the following third-party recall company: Sedgwick Brand Protection (formerly Stericycle)
Sedgwick, Memphis, TN 38120 sedgwick@sedgwick.com. from May 10, 2022 continuing through July 21, 2022.
Letter states:
If you have further distributed this product, please notify your patients at once of this product recall.
Your notification to your patients may be enhanced by including a copy of this recall notification letter.
¿ This recall should be carried out to the user level. Your assistance is appreciated and necessary to
prevent possible patient harm.
¿ Please complete and return the enclosed response form as soon as possible even if you do not have
any product on hand.
¿ Customers should contact Sedgwick directly by phone at 1-888-943-2401 to return the recalled products or if they have additional questions regarding this notification. Representatives are available Monday Friday, 8:00 am 5:00 pm PT
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Quantity in Commerce |
2 Boxes |
Distribution |
US Nationwide |
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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