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The Anspach Effort, Inc. Recall: ANSPACH***MA Attachment, Straight version Custom***Rx Onl

The Anspach Effort, Inc. Recall: ANSPACH***MA Attachment, Straight version Custom***Rx Onl is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: The Anspach Effort, Inc.; Product: ANSPACH***MA Attachment, Straight version Custom***Rx Only*** This device is intended to be used with Anspach Sy

Recalling firmThe Anspach Effort, Inc.
ProductANSPACH***MA Attachment, Straight version Custom***Rx Only*** This device is intended to be used with Anspach Systems
Reason for recallThe Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements.
ClassificationClass II (moderate — may cause temporary or reversible health consequences)
StatusTerminated
DistributionWorldwide Distribution - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden. .
Recall initiated20121128
Recall numberZ-1883-2014
Categorydevice
StateFL
CountryUnited States

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