Waldemar Link GmbH & Co. KG (Mfg Site) recalls

Waldemar Link GmbH & Co. KG (Mfg Site) has 65 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 19 Aug 2026. 62 are still ongoing. 17 were reported in the last 12 months.

Total recalls65since 2019
Last 12 months17reported
Class I00% of total
Ongoing62latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 65 100%Class III 0 0%

Why waldemar link gmbh & co. kg (mfg site) is recalled

By year

Ongoing waldemar link gmbh & co. kg (mfg site) recalls

62 active

All waldemar link gmbh & co. kg (mfg site) recalls, newest first

65 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEndo-Model, Replacement Set, Tibial Plateau, right/left, L, Uhmwpe recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherIN
DeviceCLASS IIEmbrace Drill Tower, Standard/Lateral recalledWaldemar Link GmbH & Co. KG (Mfg Site)Other15 states
DeviceCLASS IIEmbrace Drill Tower, Wedged recalled by Waldemar Link GmbH & Co. KGWaldemar Link GmbH & Co. KG (Mfg Site)Other15 states
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-0027/16 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-0027/12 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-8521/11 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-8521/09 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model SL Connection Component incl. PE-Plateau; Item Number recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-2836/11 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model SL Connection Component incl. PE-Plateau; Item Number recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-2835/12 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-0027/15 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-8521/15 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model SL Connection Component incl. PE-Plateau; Item Number recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-8030/12 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo-Model Replacement Plateau; Item Number: 15-0027/11 recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherAL, GA, TX
DeviceCLASS IILinkSymphoKnee System, Tibial Component, Modular, Symmetric recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIPlastic Trial Head Brown neck length recalledWaldemar Link GmbH & Co. KG (Mfg Site)Foreign MaterialNationwide
DeviceCLASS IIProsthesis Head B neck length recalled by Waldemar Link GmbH & Co. KGWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIL-Shaped Femoral Augment recalled by Waldemar Link GmbH & Co. KGWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIDistal Femoral Augment recalled by Waldemar Link GmbH & Co. KGWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IITibial Augment recalled by Waldemar Link GmbH & Co. KGWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIPosterior Femoral Augment recalled by Waldemar Link GmbH & Co. KGWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIModular Stem cylindrical, Tilastan¿, press-fit cementless recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIModular Stem cylindrical, Tilastan¿, press-fit cementless recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIModular Stem cylindrical, Tilastan¿, press-fit cementless recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IILINK MP Reconstruction System Neck Segment recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo Model M Tibial Components Modular Knee Prosthesis System. recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide
DeviceCLASS IIEndo Model SL Tibial Components 16-2817/02 Tibial Component, Small recalledWaldemar Link GmbH & Co. KG (Mfg Site)OtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.