3M Company Health Care Business 3m Center 3M Durapore Surgical Tape, Catalog Number 1538-118 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
3M Durapore Surgical Tape, Catalog Number 1538-118
Brand
3M Company Health Care Business 3m Center
Lot Codes / Batch Numbers
UDI/DI 50707387793208, Lot Codes: 33DER3, 33DTMA, 33DTPN, 33EDDE, 33ETFA, 33ETHX, 33FDHA, 33FDYN, 33FE9D, 33FEY6, 33FTLA, 33FW6E, 33FWPC, 33JE7T, 33JEFK, 33JENC, 33JYPX, 33JYW5, 33K3EJ, 33KPWT, 33KT6R, 33KT8F, 33LJWC, 33LK5M, 33LLEY, 33LLPT, 33LM6R, 33LMET, 33LMX3, 33N56W, 33N5K4, 33N5TC, 33NF36, 33NF6A, 33NY98, 33NYP9, 33P37P, 33PKLN, 33PL6J, 33PMFA, 33R35M, 33R3P6, 33RMNF, 33RNP4, 33TL39, 33TL8F, 33TLF4, 33TN55, 33WEA8, 33WEHJ, 33WERX, 33WF5P, 33WFD5
Products Sold
UDI/DI 50707387793208, Lot Codes: 33DER3, 33DTMA, 33DTPN, 33EDDE, 33ETFA, 33ETHX, 33FDHA, 33FDYN, 33FE9D, 33FEY6, 33FTLA, 33FW6E, 33FWPC, 33JE7T, 33JEFK, 33JENC, 33JYPX, 33JYW5, 33K3EJ, 33KPWT, 33KT6R, 33KT8F, 33LJWC, 33LK5M, 33LLEY, 33LLPT, 33LM6R, 33LMET, 33LMX3, 33N56W, 33N5K4, 33N5TC, 33NF36, 33NF6A, 33NY98, 33NYP9, 33P37P, 33PKLN, 33PL6J, 33PMFA, 33R35M, 33R3P6, 33RMNF, 33RNP4, 33TL39, 33TL8F, 33TLF4, 33TN55, 33WEA8, 33WEHJ, 33WERX, 33WF5P, 33WFD5
3M Company Health Care Business 3m Center is recalling 3M Durapore Surgical Tape, Catalog Number 1538-118 due to Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were incorrectly labeled with a shelf life of 5 years, rather than 3 years.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were incorrectly labeled with a shelf life of 5 years, rather than 3 years.
Recommended Action
Per FDA guidance
3M issued an URGENT: Voluntary Product Recall to its consignees on 03/20/2024 via email and USPS certified mail. The notice explained the issue and requested the following: Identify all affected lots in inventory (bulk) or built into kits, including kits that have been distributed. Bulk inventory: use Appendix 1 to determine the correct expiration dates to use when building kits. a. If the affected product in inventory is within the correct expiration date for the affected product correct the expiration date on the bulk package label and ensure future kits reflect the correct expiration date for the 3M affected product. b. If the affected product in inventory exceeds the correct expiration date, please destroy per facility policy. 3. Kits: Review the affected 3M lots that have been built into kits. Using Appendix 1 to determine the correct expiration date for each lot, assess if the expiration date of the kit is within the correct expiration date for the affected product. a. If the kit was labeled within the correct expiration date for the affected product, no action is required for kits in inventory nor for any kits you have distributed. b. If the kit was labeled with an expiration date exceeding the correct expiration date of the affected product, action is required. i. Kit inventory: Take action to rectify the expiration date of the kit according to the correct expiration date of the affected product or destroy the kits per facility policy. ii. Kits that have been distributed: If you have distributed kits labeled with an expiration date exceeding the correct expiration date of the affected product, please notify the impacted customers of this issue and FDA of your intent to recall/correct the affected kits. To request replacement product for the destroyed 3M Durapore Surgical Tape, Catalog Number 1538-118 product, contact 3M Health Care Customer Helpline to submit all replacement requests by calling 1-800-228-3957, option #7, or by email to 3MF
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 noticePage updated: Jan 10, 2026