Zimmer Surgical recalls

Zimmer Surgical has 26 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 8 Jul 2026. 7 are still ongoing. 5 were reported in the last 12 months.

Total recalls26since 2013
Last 12 months5reported
Class I00% of total
Ongoing7latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 25 96%Class III 1 4%

Why zimmer surgical is recalled

By year

Ongoing zimmer surgical recalls

7 active

All zimmer surgical recalls, newest first

26 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IISterile Tourniquet Hoses A.T.S¿ 4000 TS Tourniquet Systems recalledZimmer SurgicalSterilityNationwide
DeviceCLASS IISterile Tourniquet Hoses A.T.S¿ 4000 TS Tourniquet Systems recalledZimmer SurgicalSterilityNationwide
DeviceCLASS IIZimmer Tourniquet Systems A.T.S.¿ 5000TS Tourniquet Systems recalledZimmer SurgicalDevice MalfunctionOH
DeviceCLASS IIZimmer Tourniquet Systems A.T.S.¿ 3200TS Tourniquet Systems recalledZimmer SurgicalDevice MalfunctionOH
DeviceCLASS IIZimmer Dermatome recalled by Zimmer SurgicalZimmer SurgicalOtherOH
DeviceCLASS II3:1 Dermacarrier, Model Number 00219501300, skin graft carrier recalledZimmer SurgicalOtherNationwide
DeviceCLASS IIZimmer Dermatome Blades- boxes of blades recalled by Zimmer SurgicalZimmer SurgicalOtherNationwide
DeviceCLASS IIZimmer Sterile Disposable Tourniquet Cuff recalled by Zimmer SurgicalZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer Biomet Alvarado Knee Holder Base Plate Assembly recalledZimmer SurgicalForeign MaterialNationwide
DeviceCLASS IIZimmer Dermatone recalled by Zimmer SurgicalZimmer SurgicalOther17 states
DeviceCLASS IIA.T.S. 2200TS Tourniquet Systems recalled by Zimmer SurgicalZimmer SurgicalOtherNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Handpiece Loaner recalled by Zimmer SurgicalZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Width Plate recalled by Zimmer SurgicalZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Width Plate Part #00 recalledZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Handpiece recalled by Zimmer SurgicalZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Width Plate Part #00 recalledZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Width Plate Part #00 recalledZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Handpiece w/o Hose recalled by Zimmer SurgicalZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIZimmer¿ Air Dermatome II Width Plate Part # recalled by Zimmer SurgicalZimmer SurgicalPackaging DefectsNationwide
DeviceCLASS IIDual Port/Single Bladder Disposable Tourniquet Cuff recalledZimmer SurgicalOther45 states
DeviceCLASS IIDual Port/Single Bladder Disposable Tourniquet Cuff recalledZimmer SurgicalOther45 states
DeviceCLASS IIIZimmer Hemovac Device Hemovac Mini Evacuator recalled by Zimmer SurgicalZimmer SurgicalPackaging Defects8 states
DeviceCLASS IIUniversal Modular Electric/Battery Handpiece recalled by Zimmer SurgicalZimmer SurgicalDevice MalfunctionNationwide
DeviceCLASS IIZimmer Air Dermatome II recalled by Zimmer SurgicalZimmer SurgicalOtherNationwide
DeviceCLASS IIThe Zimmer Air Dermatome recalled by Zimmer SurgicalZimmer SurgicalOtherNationwide
DeviceCLASS IIZimmer Air Dermatome II recalled by Zimmer SurgicalZimmer SurgicalOtherNationwide

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.