The Anspach Effort recalls

The Anspach Effort has 260 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 18 Jan 2023. 10 are still ongoing.

Total recalls260since 2012
Last 12 months0reported
Class I21% of total
Ongoing10latest 18 Jan 2023

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 2 1%Class II 258 99%Class III 0 0%

Why the anspach effort is recalled

By year

Ongoing the anspach effort recalls

10 active

All the anspach effort recalls, newest first

260 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAdult Craniotome recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIAdult Rotating Craniotome Attachment recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIAdult Craniotome, Thin Foot Plate Attachment recalledThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIAdult Rotating Craniotome Attachment recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IILarge Craniotome Attachment Use with XMax¿, microMax recalledThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIPediatric Craniotome Attachment recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IILarge Rotating Craniotome Attachment recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIAdult Craniotome, Large recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIPediatric Craniotome recalled by The Anspach EffortThe Anspach EffortProcessing DeviationNationwide
DeviceCLASS IIOscillating Saw Attachment Surgical instrument motors recalledThe Anspach EffortOtherFL
DeviceCLASS IIAutolube-III Product Usage: Pneumatic system recalledThe Anspach EffortOtherNationwide
DeviceCLASS IIPediatric Craniotome, Bm recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIBearing Sleeve Curved recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIAl-iii W/ male disconnect and 20ft hose recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIAttachment, Black Max recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIImri Short Hd Attachment recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIMedium Attachment recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIOtologic Curved Micro recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIAdlt Crani, Thin Ft Plate recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIBearing Sleeve Straight Taper recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIMinimally Invasive Attachment recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIMinimal Access Attachment recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIMinimal Access Attachment, Black MAX recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IISagittal Saw recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIAttachment, Black Max recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIConsole, eMax2 Plus recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIChuck Driver System recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IISmall Attachment, Jacobs Chuck recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIMinimal Access Straight Driver recalled by The Anspach EffortThe Anspach EffortOtherNationwide
DeviceCLASS IIB-sagittal Assembly recalled by The Anspach EffortThe Anspach EffortOtherNationwide

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.