DeRoyal Industries Inc DeRoyal BREAST TRAY, REF 89-7033.07 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DeRoyal BREAST TRAY, REF 89-7033.07
Brand
DeRoyal Industries Inc
Lot Codes / Batch Numbers
Lot Numbers: Lot 56390335 exp 1/1/2024, Lot 57001021 exp 1/1/2024
Products Sold
Lot Numbers: Lot 56390335 exp 1/1/2024; Lot 57001021 exp 1/1/2024
DeRoyal Industries Inc is recalling DeRoyal BREAST TRAY, REF 89-7033.07 due to XXX. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
XXX
Recommended Action
Per FDA guidance
The firm issued an URGENT RECALL NOTICE to its consignees on 11/03/2022 by email and US mail. 1) Using the attached Affected Products Listing Spreadsheet, identify affected part/lot numbers in your inventory and place in quarantine to prevent further use. 2) DeRoyal will contact you to schedule time to affix labels to all affected product. These labels indicate that, at the time of use, the affected product should be removed from the kit/tray and destroyed. These products should be destroyed according to your facility, local, state and federal regulations. 3) DeRoyal representative will determine kits/trays and affected lot numbers which require the labeling indicating to remove 3M Health Care item. 4) The completed the NOTICE OF DESTRUCTION FORM shall be emailed to recalls@deroyal.com no later than 12/8/2022. PLEASE COMPLETE THIS FORM EVEN IF YOU NO LONGER HAVE ANY INVENTORY. 5) The remaining items in the kit/tray are unaffected and may still be used. Distributors were asked to perform the following: "1) Using the attached Distributor Affected Products Listing Spreadsheet, identify affected part/lot numbers in your inventory and request placement in quarantine to prevent further use. 2) Please notify us with the quantity of affected cases, product and lot numbers in your inventory to which labels will need to be applied. Email this to recalls@deroyal.com no later than 11/21/2022. We will immediately send labeling for you to apply to case and each pack contained within. 3) These labels indicate that, at the time of use, the affected product should be removed from the kit / tray and destroyed. 4) The remaining items in the kit/tray are unaffected and may still be used. 5) If you have questions or need assistance with the recall, please contact your DeRoyal Supplier Relations contact, customer service at 888.938.7828, or email us at recalls@deroyal.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, CT, FL, GA, IL, IN, KS, LA, MA, MI, MN, MS, MO, NJ, NY, NC, OH, PA, TN, TX, VA, WI
Page updated: Jan 10, 2026