Z-0241-2016Class II

DeRoyal Sterile Custom Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical Solution, Catalog...

Name: Z-0241-2016 DeRoyal Sterile Custom Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical Solution, Catalog...
Creator: DeRoyal Industries Inc
Published: 2015-08-31
License: https://open.fda.gov/license/

DeRoyal Industries, Inc. / initiated 2015-08-31 / Terminated / root cause: packaging

FDA source

DeRoyal Industries Inc began a recall of DeRoyal Sterile Custom Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical Solution, Catalog No. 8630, Lot Nos: 2016-09EE or 2016-09EF, or... on 2015-08-31. FDA classified it as Class II and gives the reason as "Custom Sterile Surgical kits contain 3M DuraPrep (TM) Surgical Solution, Catalog Number 8630, Lot Number 2016-09EE which was recalled due to unintended exposure to the sterilant during package sterilization". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0241-2016
Classification: Class II
Status: Terminated
Initiated: 2015-08-31
Posted: 2015-11-06
Terminated: 2016-04-12
Recalling firm: DeRoyal Industries, Inc.
Product: DeRoyal Sterile Custom Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical Solution, Catalog No. 8630, Lot Nos: 2016-09EE or 2016-09EF, or 2016-09EG, or Catalog No. 863, Lot No. 2016-08DC: TOTAL JOINT PACK A&B, REF 89-5720.04; PACEMAKER PACK, REF 89-6717.03
Product code: LRO General Surgery Tray
Reason for recall: Custom Sterile Surgical kits contain 3M DuraPrep (TM) Surgical Solution, Catalog Number 8630, Lot Number 2016-09EE which was recalled due to unintended exposure to the sterilant during package sterilization.
Root cause tag: packaging
FDA root cause: Other
Action: DeRoyal initiated their recall on 08/31/2015 to the end-user level by sending overnight letters to its direct accounts and hospitals. Distributors were asked to put the product in quarantine, place the provided labels on the products and complete and return the spreadsheet of how many they labeled. They were asked to return the spreadsheet even if they did not have inventory. Hospitals were provided with labels to affix to the kits with direction to discard the recalled component and notice of destruction forms to be completed and returned.
Distribution: SC, FL, OH, NJ, OK, MN, AR
Product codes and lots: REF 89-5720.04, Lot Number 38322988; REF 89-6717.03, Lot Numbers: 38323059 and 38342436

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0241-2016
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0240-2016	Class II	Terminated	Voluntary: Firm initiated	2015-11-18	2015-11-06
Z-0241-2016	Class II	Terminated	Voluntary: Firm initiated	2015-11-18	2015-11-06

Product code LRO

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-14, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)