Z-0654-2014 Class II Terminated
FDA device recall Z-0654-2014 was initiated by The Anspach Effort, Inc. on Apr 25, 2013 and is designated Class II. Reason for recall: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary removal of the Pneumatic Drill System, including the motor hand-piece, Auto Lube foot control, without a pressure relief valve… The recall status is terminated (terminated Jul 20, 2015). Affected quantity: 2,785.
Recall Details
- Product Type
- Devices
- Report Date
- Jan 15, 2014
- Initiation Date
- Apr 25, 2013
- Termination Date
- Jul 20, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,785
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution: US (nationwide) including Puerto Rico and states of: AL, AR, AZ, CA, CO, CT, DC, DE, GA, FL, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VE, VT, WA, WI, WY, and WV. Internationally to: AT, AU, BR, BS, CA, CH, CL, CO, CZ, CR, DE, DK, DO, EG, ES, FI, FR, GB, GR, HK, HU, ID, IL, IN, IS, JP, KH, KR, LB, LT, MX, MY, NL, NO, NZ, PA, PE, PH, PL, PT, SA, SG, SY, TH, TR, TW, and ZA.
Code Information
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0654-2014
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026