FDA Medical Device Recalls (openFDA)
Olympus Corporation of the Americas: BF-MP160F: EVIS EXERA Bronchofibervideoscope
- Recall number
- Z-1048-2022
- Recalling firm
- Olympus Corporation of the Americas
- Product
- BF-MP160F: EVIS EXERA Bronchofibervideoscope
- Status
- Open, Classified
- Initiated
- 2022-03-08
- Posted
- not on file
- Terminated
- not on file
- Reason
- Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization
- Root cause
- Other
- Action
- Olympus issued Urgent Medical Device Correction Letters on 3/8/22. Letter states reason for recall, health risk and action to take: 1. Inspect your inventory for the referenced devices and identify any device with the model names specified above. Please check all areas of the hospital to determine if any of these devices remain in inventory. 2. Carefully read the content of this Medical Device Correction Action as well as the attached Addendum . The addendum provides updated information or instructions on the chemicals to be used for reprocessing, the sterilization conditions, rinsing after high-level disinfection, and a recommendation on using sterilization. 3. Ensure all personnel are completely knowledgeable and thoroughly trained on the new reprocessing steps. 4. Additional copies of the new Operation Manuals can be obtained by accessing our OlympusConnect site and downloading a copy of the new Manuals. Please visit our OlympusConnect customer website: at https://www.OlympusConnect.com. New users will need to register. Once registered select [Product Support] on the left navigation bar, then select [Instruction Manuals], locate the BF-XT160, BF-XP160F, BF-MP160F and BF-3C160 and select the [Download] option. 5. Access the Olympus portal to indicate that you have received this notification. Go to https://olympusamerica.com/recall. Enter the reference number 0405 and provide your contact information as indicated in the portal. 6. If you have further distributed this product, identify your customers, forward them this notification, and appropriately document your notification process. Contact our Technical Assistance Center (TAC) at 1-800-848-9024, option 1. The TAC department can assist in answering questions on BF-XT160, BF-XP160F, BF-MP160F and BF-3C160 bronchoscope cleaning and reprocessing. " Olympus America has dedicated field personnel, called Endoscopy Support Specialists, who visit customer sites to assess and observe customer reprocessing methods and to
- Quantity
- 292 units
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- All serial numbers. UDI: 04953170289064
- 510(k) numbers
- ["K033225"]
- PMA numbers
- not on file
- Product code
- EOQ
- Firm FEI
- 2429304
- Firm city
- Center Valley
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28