# China NMPA Product Recall - Anspach Micromax Pneumatic Drill

Source: https://www.globalkeysolutions.net/records/china_product_recall/the-anspach-effort-inc/14636b5b-4b2f-41ed-ad05-d91e1add719e/
Source feed: China

> China NMPA product recall for Anspach Micromax Pneumatic Drill by The Anspach: Effort, Inc. published September 18, 2017. Recall level: Level 3 Recall. The AnspachEffort, Inc., a medical device manufacturer represented by Johnson & Johnson (Shanghai) M

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: The AnspachEffort, Inc. is voluntarily recalling its pneumatic bone surgery equipment.
- Company Name: The Anspach: Effort, Inc.
- Publication Date: 2017-09-18
- Product Name: Anspach Micromax Pneumatic Drill
- Recall Level: Level 3 Recall
- Recall Reason: The accompanying product instructions do not include a recommended maintenance period.
- Discovering Company: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd.
- Manufacturing Company: The Anspach: Effort, Inc.
- Summary: The AnspachEffort, Inc., a medical device manufacturer represented by Johnson & Johnson (Shanghai) Medical Devices Co., Ltd., initiated a voluntary Class III recall of its Anspach Micromax Pneumatic Drill. This recall was formally reported on August 7, 2017, and publicly noted by the National Medical Products Administration (NMPA) on September 18, 2017. The primary concern was the omission of a recommended maintenance period from the device's instructions for use (DFU), specifically for pneumatic bone surgery devices shipped after September 28, 2015. This constitutes a regulatory non-compliance in product documentation. Although a global recall was initiated by AnspachEffort, Inc., the 

Company: https://www.globalkeysolutions.net/companies/the-anspach-effort-inc/02a6764e-eb0b-4899-89b3-11e4f3cbcafc/