Recall Z-0094-2019
Widex A/S · initiated August 31, 2018
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10 Intended use: BABY440 is intended for, but not limited to, babies (0 to 3 years of age) to be used as air conduction amplification devices in everyday listening environments.
Codes / lots: Serial numbers 024569 and 024550
Reason for recall
The reason for this field action is due to the mounting of a non-tamper-resistant (ordinary) battery drawer on some BABY440 hearing aids. The correct battery drawer is tamper-resistant and require a special tool to open it.
FDA-determined cause: Employee error
Action taken
The firm, Widex, sent an "Urgent Medical Device Correction Letter" dated 8/28/18 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to do the following: a) Investigate, whether your childs BABY440 hearing aid is mounted with the correct battery drawer. Please refer to the attachment How to determine if correct battery drawer is mounted. b) If affirmative, return the product to the hearing care professional, where you bought the hearing aid, to have the tamper-resistant battery drawer mounted. If you have any questions, contact Director, Global Regulatory Affairs at 0045 44 35 57 71 or email to: krpe@widex.com.
Details
- Recall number
- Z-0094-2019
- Initiated
- August 31, 2018
- Terminated
- December 21, 2018
- Product code
- ESD – Hearing Aid, Air-Conduction, Prescription
- Quantity
- 2
- Distribution
- US Distribution to states of: GA and NY.
- Recalling firm
- Widex A/S, Lynge