RecallDepth

Grafton DBM Orthoblend, Model Numbers: a) T44125INT, b) T44135, c) T44145, d) T44150; Demineralized Bone Matrix

Company
Medtronic Sofamor Danek Usa Inc
Recall Initiated
September 26, 2023
Posted
October 25, 2023
Recall Number
Z-0165-2024
Quantity
430 units
Firm Location
Memphis, TN

Reason for Recall

Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.

Distribution

US, Colombia, S. Korea, New Zealand, India, Taiwan

Lot / Code Info

a) T44125INT: GTIN 00643169965058, Serial Numbers: A52559-042, A52559-024, A52559-038, A52559-039, A52559-040, A52559-041, A52559-044, A52559-045, A52559-021, A52559-022, A52559-023, A52559-025, A52559-026, A52559-027, A52559-028, A52559-029, A52559-030, A52559-031, A52559-032, A52559-033, A52559-034, A52559-035, A52559-036, A52559-037, A52559-043; b) T44135: GTIN 00643169122918, Serial Numbers: A59102-034, A59102-035, A58789-025, A58789-026, A58789-027, A59080-036, A59080-037, A58789-030, A58789-031, A58789-032, A58789-033, A58789-034, A58789-035, A58789-036, A58789-037, A58789-038, A58789-039, A59102-042, A59102-043, A59102-044, A59102-045, A59102-046, A59102-047, A59102-048, A59102-049, A59102-050, A59102-051, A59103-030, A59103-031, A59103-032, A59103-033, A59103-034, A59103-035, A59103-036, A59103-037, A59103-038, A59103-039, A59102-055, A59102-056, A58789-061, A58789-062, A59080-022, A59080-026, A59080-027, A59080-028, A59080-029, A59080-030, A59102-038, A59102-039, A59102-040, A59102-041, A59102-059, A59102-060, A59102-061, A59102-062, A58789-047, A59103-042, A59103-043, A59103-044, A59103-045, A59103-046, A58789-028, A58789-029, A59080-020, A59080-021, A59080-023, A59102-031, A59102-032, A59102-033, A59080-024, A59080-025, A59102-029, A59103-040, A59080-031, A59080-016, A59080-017, A58789-042, A58789-043, A58789-044, A58789-045, A58789-046, A58789-048, A58789-049, A58789-021, A58789-022, A58789-023, A59080-019, A59102-057, A59102-058, A59103-041, A58789-050, A58789-054, A58789-055, A58789-056, A58789-057, A58789-058, A58789-059, A58789-060, A59103-016, A59103-017, A59103-018, A59103-029, A59080-018, A59102-028, A59102-030, A59102-052, A59102-053, A59102-054; c) T44145: GTIN 00643169122925, Serial Numbers: A56911-076, A56911-070, A56911-071, A56911-023, A56911-067, A47028-065, A56911-082, A59197-041, A59197-059, A56911-074, A56911-075, A47028-053, A57248-034, A56911-018, A59197-057, A59197-036, A59197-037, A59197-020, A59197-021, A59197-022, A59197-023, A59197-024, A56911-028, A56911-029, A56911-030, A56911-031, A56911-033, A57248-039, A56911-034, A56911-035, A56911-080, A59197-034, A56911-077, A56911-078, A56911-079, A59197-047, A59197-044, A56911-068, A56911-044, A56911-045, A56911-046, A56911-081, A57248-020, A57248-032, A57248-036, A59197-062, A56911-032, A59197-055, A59197-051, A59197-052, A57248-025, A57248-026, A57248-027, A57248-028, A57248-029, A56911-041, A59197-048, A56911-020, A56911-024, A56911-025, A56911-047, A56911-048, A56911-049, A56911-050, A56911-051, A56911-052, A56911-053, A56911-054, A56911-055, A56911-056, A56911-057, A56911-058, A56911-042, A56911-043, A56911-072, A56911-073, A57248-013, A57248-014, A47028-036, A47028-037, A47028-038, A56911-059, A47028-039, A56911-027, A47028-040, A59197-011, A59197-012, A59197-013, A47028-059, A57248-033, A59197-018, A59197-019, A47028-066, A47028-067, A59197-049, A59197-050, A47028-041, A47028-042, A59197-040, A47028-043, A47028-044, A57248-011, A57248-012, A59197-025, A59197-026, A59197-027, A59197-028, A59197-029, A59197-030, A59197-031, A59197-032, A59197-033, A56911-019, A56911-021, A56911-022, A56911-060, A56911-061, A56911-062, A56911-063, A56911-064, A56911-065, A56911-066, A57248-030, A57248-031, A57248-035, A59197-038, A59197-039, A59197-060, A59197-061, A57248-038, A59197-054, A47028-045, A47028-046, A47028-047, A47028-048, A59197-014, A59197-015, A59197-016, A59197-017, A56911-069, A59197-045, A57248-015, A57248-016, A57248-017, A57248-018, A56911-036, A56911-037, A56911-038, A56911-039, A56911-040, A47028-049, A47028-050, A47028-051, A47028-052, A57248-037, A59197-064, A59197-065, A47028-054, A59197-042, A59197-043, A59197-053, A56911-026, A59197-056, A57248-019, A47028-055, A47028-056, A59197-046, A59197-063, A59197-058, A47028-057, A47028-058, A59197-035; d) T44150: GTIN 00643169122932, Serial Numbers: A48245-164, A48245-168, A57914-011, A57914-012, A57914-023, A57914-024, A57914-025, A59191-061, A59191-058, A58758-035, A58758-036, A58758-037, A58758-059, A59191-038, A59191-039, A58758-034, A58758-038, A59191-040, A48245-121, A48245-122, A48245-123, A48245-124, A48245-147, A48245-148, A48245-149, A48245-160, A48245-170, A58758-060, A58758-061, A58758-062, A59191-062, A59191-063, A59191-064, A58758-039, A57914-013, A57914-014, A57914-015, A57914-016, A57914-017, A58758-040, A58758-041, A58758-042, A59191-041, A58758-043, A58758-044, A48245-165, A48245-166, A48245-167, A48245-169, A58758-045, A58758-046, A58758-050, A58758-051, A58758-047, A58758-048, A58758-049, A59191-042, A59191-043, A59191-044, A58758-031, A58758-032, A58758-033, A59191-045, A59191-046, A59191-047, A59191-048, A59191-049, A48245-135, A48245-136, A48245-137, A48245-138, A48245-139, A48245-140, A48245-141, A48245-142, A48245-143, A48245-144, A48245-145, A48245-146, A48245-150, A48245-151, A48245-152, A48245-153, A48245-154, A48245-155, A48245-156, A48245-157, A57914-018, A57914-019, A57914-020, A57914-021, A57914-022, A48245-161, A48245-125, A48245-126, A48245-127, A48245-128, A48245-129, A48245-130, A48245-131, A48245-132, A48245-133, A48245-134, A48245-158, A48245-159, A48245-162, A59191-050, A59191-051, A48245-163, A58758-052, A59191-052, A59191-053, A58758-063, A59191-060, A58758-053, A58758-054, A58758-055, A59191-054, A59191-055, A59191-059, A58758-056, A58758-057, A58758-058, A59191-056, A59191-057

Root Cause

Employee error

Action Taken

Medtronic issued an URGENT: MEDICAL PRODUCT RECALL notice to its consignees on 09/26/2023 via UPS 2-day delivery. The notice explained the problem, potential risk, and requested the return of the affected devices.

More recalls by Medtronic Sofamor Danek Usa Inc

View all recalls by this company →