RecallDepth

EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03; b. EZ Derm 7 x 18 (17 x 46 cm) Non-Perforated, Part Number: 131704-03; c. EZ Derm 2 x 2 (5 x 5 cm) Non-Perforated, Part Number: 131705-03; d. EZ Derm 3 x 48 (8 x 122 cm) Perforated, Part Number: 131710-03; e. EZ Derm 3 x 24 (8 x 61 cm) Perforated, Part Number: 131711-03; f. EZ Derm 3 x 12 (8 x 30 cm) Perforated, Part Number: 131712-03; g. EZ Derm 3 x 4 (8 x 10 cm) Perforated, Part Number: 131713-03; h. EZ Derm 7 x 18 (17 x 46 cm) Perforated, Part Number: 131714-03; i. EZ Derm 2 x 2 (5 x 5 cm) Perforated. Part Number: 131715-03 Product Usage: EZ Derm is a porcine derived xenograft in which the collagen has been cross linked with an aldehyde. EZ Derm (porcine xenograft) can be used for partial thickness skin loss injuries. Use of EZ Derm for burns, donor sites and chronic vascular ulcers reduces pain and fluid loss. EZ Derm can also be used as a temporary cover, or test graft, prior to auto grafting and as a protective covering over perforated auto grafts.

Company
Molnlycke Health Care, Inc
Recall Initiated
March 26, 2019
Terminated
June 2, 2021
Recall Number
Z-1243-2019
Quantity
1,332 units
Firm Location
Norcross, GA

Reason for Recall

Intermittent heat seal failures on the outer pouch of some EZ Derm products.

Distribution

Worldwide Distribution - US Nationwide distribution to AL, AZ, CA, CO, DC, FL, GA, IA, IL, KS, LA, MA, MD, MN, MO, NC, NE, NJ, OK, PA, RI, TN, TX, VA, WA, WI. International distribution to Chile, Jamaica.

Lot / Code Info

a. Part Number: 131703-03, Lot Numbers: 18418740, 18489748, 18489749, 18489750, 18497584, 18515343, 18515344, 19010755, 19011801, 19024014, 19024015, 19024017, 19027570, 19034016, 19041030, 19054457;   b. Part Number: 131704-03, Lot Numbers: 18489747, 19041029;   c. Part Number: 131705-03, Lot Numbers: 18409561, 18411794, 18421375, 18421378, 18448600, 18457912, 18458926, 18460179, 18489746, 18497582, 18497583, 18505338, 18505339, 18505340, 19033438, 19033439;   d. Part Number: 131710-03, Lot Numbers: 18409559, 18411793, 18421334, 18421377, 18435885, 18448598, 18453214, 18453297, 18453300, 18453303, 18505328, 18505329, 18505330;   e. Part Number: 131711-03, Lot Number 18409562;   f. Part Number: 131712-03, Lot Numbers: 18409557, 18411791, 18418739, 18421332, 18429844, 18435028, 18435029, 18448582, 18448596, 18458925, 18460132, 18460145, 18460174, 18460175, 18470176, 18489702, 18489703, 18489704, 18489745, 18497579, 18497580, 18497581, 18505332, 18505333, 18505334, 18515336, 18515337, 19024010, 19024011, 19024013, 19033435, 19034012;   g. Part Number: 131713-03, Lot Numbers: 18411792, 18421333, 18421376, 18429855, 18435030, 18435031, 18435032, 18448584, 18448597, 18448599, 18453295, 18453298, 18453301, 18460133, 18460146, 18460177, 18470178;   h. Part Number: 131714-03, Lot Numbers: 18409555, 18411790, 18418738, 18421331, 18435025, 18435026, 18448583, 18448595, 18460130, 18460134, 18460171, 18460172, 18470173, 18489699, 18489700, 18489701, 18497576, 18497577, 18497578, 18515341, 18515342, 19010584, 19024006, 19024007, 19024009, 19033234, 19033441, 19034008, 19041077, 19041080, 19054456;   i. Part Number: 131715-03, Lot Numbers: 18435886, 18453296, 18453299, 19041079, 19041081

Root Cause

Equipment maintenance

Action Taken

Molnylcke notified consignees on about 03/26/2019 via "URGENT FIELD SAFETY NOTICE" letter. Consignees were instructed to review current inventory for affected devices, separate and discard affected devices, complete and return the Confirmation Form, and replacement product will be provided or credit issue after receipt of the completed Confirmation Form. If product was further distributed, consignees were instructed to forward a copy of the Field Safety Notice with the Confirmation Form and request that they return the Confirmation Form to them and send their reconciliation results to Molnlycke. Questions or comments can be directed to Molnlycke Customer Service at 1-800-843-8497 or your Account Manager/Sales Representative.

More recalls by Molnlycke Health Care, Inc

View all recalls by this company →