RecallRadar

FDA Device recall Z-0718-2014

Anspach Single Use Sterile Bone Cutting Burs and Irrigation Clips

On 2014-01-22 the FDA classified a Class II recall of Anspach Single Use Sterile Bone Cutting Burs and Irrigation Clips by The Anspach Effort, citing recall was initiated due to the observation of separation between clear layers of the pouch during real time aging studies. As a result, it is possible to have a breach in the ste….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0718-2014
ClassificationClass II
Statusterminated
Initiated2011-09-09
Published2014-01-22
Last updated2026-09-13 11:53 UTC
CompanyThe Anspach Effort
DistributionUS

Product

Anspach Single Use Sterile Bone Cutting Burs and Irrigation Clips. Rx Only

Reason

Recall was initiated due to the observation of separation between clear layers of the pouch during real time aging studies. As a result, it is possible to have a breach in the sterile barrier.

Identifiers

code_info
A-CRN B123005578 LHD-6AC 8123005628 Q08-4B 311838 5-6R 333195 A-CRN B143006072 LH0-6AC 8393012282 QD8-4B 312583 S-6R 3…A-CRN B123005578 LHD-6AC 8123005628 Q08-4B 311838 5-6R 333195 A-CRN B143006072 LH0-6AC 8393012282 QD8-4B 312583 S-6R 333458 A-CRN B183006882 LHD-6AC (463028357 Q08-4B 315793 S-6R 333793 A-CRN B213007929 LHD-6AC 8423013160 QD8-4B 316956 S-6R 333982 A-CRN 8313010424 LHD-6AC (253022922 QD8-48 317934 S-6R 334093 A-CRN 8373011925 LHD-6AC B073004408 008-48 318394 S-6R 334236 A-CRN 8393012268 LHD-6AC B373011840 Q08-48 319435 S-6R 334455 A-CRN 8393012369 LHD-6AC 093020161 Q08-48 319991 5-6R 334640 A-CRN 8393012486 LHD-6AC (243022710 008-48 330615 S-6R 334925 A-CRN 8433013376 LHD-6AC (303024122 Q08-4B 331283 S-6R 335148 A-CRN 8493014144 LHD-6AC 8243008895 Q08-4B 50220710 S-6R 335723 A-CRN 8513015111 LHD-6AC (423027109 Q08-4B 50244135 S-6R 335922 A-CRN B513015587 LHD-6AC 8283009782 Q08-4B 50288181 S-6R 336059 A-CRN 8533015857 LHD-6AC 8473013675 QD8-4B 50335706 S-6R 336180 A-CRN (083017208 LHD-6AC 023018999 Q08-48 50416854 S-6R 336 A-CRN-S-4 C353025392 M-2DC 611433 Q08-58 621855 5-

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0718-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.