Zimmer Surgical Inc: Medical Device Recall in 2024 - (Recall #: Z-1078-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

Product Classification:

Class II

Date Initiated: January 2, 2024

Date Posted: February 21, 2024

Recall Number: Z-1078-2024

Event ID: 93790

Reason for Recall:

Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary.

Status: Ongoing

Product Quantity: 76 boxes (1,520 units) US; 521 boxes (10,420 units) OUS

Code Information:

UDI-DI 00889024378780 Lots 65292843 (Expires 16-Oct-2026) and 65390419 (Expires 18-Jan-2027)

Distribution Pattern:

Worldwide - US Nationwide distribution including in the states of CA, DE, FL, GA, IA, IL, IN, KS, LA, MI, MO, MT, NC, NV, NY, OH, OK, PA, RI, TN, TX, UT, VA, WA, WI, WV and the countries of AUTRALIA, CANADA, DNIPRO OBLAS, HONG KONG, INDIA, JAPAN, MEXICO, CDMX, NETHERLANDS, SEOUL KOREA, SINGAPORE, TAIWAN, THAILAND.

Voluntary or Mandated:

Voluntary: Firm initiated