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The Anspach Effort, Inc.

The Anspach Effort, Inc. Recalls

All product recalls associated with The Anspach Effort, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Dec 2022

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 30 recalls

The Anspach Effort, Inc.: 6.5 cm Pediatric Craniotome Attachment. Use with XMax, mi...

Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: Pediatric Craniotome Ref:CRANI-P-G1

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMa...

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FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: 7.5 cm Large Craniotome Attachment Use with XMax, microMa...

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: 7.5 cm Large Rotating Craniotome Attachment. Use with XMa...

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: 6.5 cm Adult Craniotome, Thin Foot Plate Attachment. Use ...

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cu...

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: Adult Craniotome Ref: CRANI-A-G1 Intended for cutting a...

FDADec 7, 2022Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: 16cm Minimally Invasive Attachment. For use with Motor S...

Customer complaint indicating the color bands on the MIA16-G1 were not correct.

Class IIModerate

FDADec 10, 2014CA, NC• The Anspach Effort, Inc.

The Anspach Effort, Inc.: Synthes Small Electric Drive (SED)

May operate solely in reverse mode, not operate in reverse mode when intended, not function or an unintentionally start.

Class IIModerate

FDANov 14, 2014AZ, AR, CA +13 more• The Anspach Effort, Inc.

The Anspach Effort, Inc.: Synthes Small Electric Drive (SED). For use in general t...

The affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start.

Class IIModerate

FDAAug 14, 2014Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: Foot Pedal, Foot Control for SC2000 and SC2100 Powered, s...

The Anspach Effort, Inc. is recalling the Foot Control/ Foot Pedal for SC2000 and SC2100 Powered, simple cranial drills, burrs, trephines, and accessories. The Foot Control Cables lacks the shield connection from the cable to the connector body. The lack of shielding may result in radiated emissions which could possibly cause interference on other electrical equipment adjacent to the foot pedal

FDAAug 13, 2009Nationwide• The Anspach Effort, Inc.