Every recall we track for The Anspach Effort, Inc. — 10 in all — plus the complaints and injury reports the public filed about them.
Anspach recalls CRANI-A-G1 craniotome attachments due to potential ball bearing dislodgement during use, risking serious patient injury if inspection intervals are not followed.
Anspach recalls 6.5 cm Adult Rotating Craniotome Attachments used with XMax, microMax, and eMax systems due to potential ball bearing dislodgement during use, which could cause serious patient injury if not inspected regularly.
Anspach recalls 6.5 cm Adult Craniotome Thin Foot Plate Attachment used with XMax, microMax, and eMax systems. Ball bearings may dislodge during use, risking serious patient injury if inspection intervals aren't followed.
Anspach recalls 6.5 cm Adult Rotating Craniotome Attachment (CRANI-A-R) used with XMax, microMax, and eMax systems. Ball bearings may dislodge during use, risking serious patient injury if not inspected per instructions.
Anspach recalls 7.5 cm Craniotome Attachment for possible ball bearing dislodgement during surgery, risking serious patient injury if not inspected regularly.
Anspach recalls 6.5 cm Pediatric Craniotome Attachment used with XMax, microMax, and eMax systems. Ball bearings may dislodge during removal, risking serious patient injury if not inspected regularly.
Anspach recalls 7.5 cm Large Rotating Craniotome Attachments used with XMax, microMax, and eMax systems due to risk of ball bearings dislodging during surgery, potentially causing serious patient injury. All units are affected.
Anspach recalls adult craniotomes (CRANI-L-G1) due to ball bearings potentially falling out during use, risking serious patient injury if not inspected regularly.
Anspach recalls pediatric craniotome Ref CRANI-P-G1 due to risk of serious injury from ball bearings dislodging during use. All units are affected. Contact for remedy.
