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U.S. Department of Health and Human Services

Class 2 Device Recall Safeguard US Operating LLC

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 Class 2 Device Recall Safeguard US Operating LLCsee related information
Date Initiated by FirmAugust 27, 2024
Date PostedSeptember 19, 2024
Recall Status1 Open3, Classified
Recall NumberZ-3183-2024
Recall Event ID 95183
Product Classification Pack, hot or cold, disposable - Product Code IMD
ProductKits of Convenience containing 1 of the 2 Item Numbers: 1. Item Number: 59-300 HAWK Warming Grid, 2. Item Number: 59-320 HAWK Advanced Hypothermia Management Set. Convenience kits labeled as follows: Combat Life Saver - Intermediate (Product Number: 83-323-CB) contains 59-300 / 1 Each; Medic Enhancement Resupply (Product Number: 82-504-05) contains 59-300 / 1 Each; Combat Life Saver - Advanced (Product Number: 83-325-CB) contains 59-300 / 1 Each; Cold Weather (Product Number: 82-505) contains 59-300 / 1 Each; HAWK w/ Carrier Set, Multicam, Stocked (Product Number: 83-315-01-MC) contains 59-300 / 1 Each; Mojo Combat Life Saver - Intermediate - Multicam (Product Number: 83-323-MC); Combat Life Saver - Intermediate - Multicam (Product Number: 83-323-MC); Mojo Combat Life Saver - Advanced - Multicam (Product Number: 83-325-MC); DIRECT ACTION BAG, FOLIAGE GREEN, ADVANCED, STOCKED (Product Number: 84-497-FG).
Code Information 1. Product Number: 83-323-CB; Lot Numbers: PBO0004044, PBO0003913, PBO0004523. 2. Product Number: 82-504-05; Lot Numbers: PBO0004123. 3. Product Number: 83-325-CB; Lot Number: PBO0004172. 4. Product Number: 82-505; Lot Number: pbo0003673. 5. Product Number: 83-315-01-MC; Lot Number: PBO0004179. 6. Product Number: 83-323-MC; Lot Number: PBO0004291, PBO0004454. 7. Product Number: 83-325-MC; Lot Number: PBO0004285. 8. Product Number: 84-497-FG; Lot Number: PBO0004817.
Recalling Firm/
Manufacturer		 Safeguard US Operating LLC
5555 Harrisburg Ind Pk Dr
Harrisburg NC 28075-7407
For Additional Information ContactKimberly Reed
855-428-6074
Manufacturer Reason
for Recall		Incorrect expiration date.
FDA Determined
Cause 2		Process control
ActionSafeguard US Operating notified customers via letters sent on 08/27/2024. Customers were instructed to remove the Convenience Kits from all points of use and return to Safeguard US Operating LLC for label correction of the HAWK component. Also complete the attached Recall Acknowledgement and Receipt Form and return it to Safeguard US Operating LLC per the instructions on the form. Distributors were instructed to carry out the recall to the consumer/user level and to identify customers who received the product and notify them of the recall, including a copy of the letter to enhance notification.
Quantity in Commerce567 units
DistributionUS Nationwide distribution in the states of AK, CA, CO, DC, GA, IL, NC, NM, NY, OK, OR, RI, TX, VA, WA, WI.
Total Product Life CycleTPLC Device Report
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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