Z-3283-2018Class II
Bronchovideoscope BF-160
OLYMPUS Corporation of the Americas / initiated 2018-08-08 / Terminated
Olympus Corporation of the Americas began a recall of Bronchovideoscope BF-160 on . FDA classified it as Class II and gives the reason as "The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port". As of , the recall status on record is Terminated.
Recall record
- Recall number
- Z-3283-2018
- Classification
- Class II
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- OLYMPUS Corporation of the Americas
- Product
- Bronchovideoscope BF-160
- Product code
- EOQ Bronchoscope (Flexible Or Rigid)
- Reason for recall
- The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
- FDA root cause
- Other
- Action
- Urgent Medical Device Safety Notice letters dated 8/8/18 were distributed to customers. The letters instructed customers to perform the following: Our records indicate that your facility has purchased one or more of the above-referenced endoscopes. OLYMPUS requires that you take the following actions: Inspect your inventory for the referenced Olympus models. Please keep this customer letter in your inventory and conduct the following action prior to every use. Step 1: Wearing sterile gloves, attempt to rotate or turn the instrument channel port in counter-clock direction as shown in picture 01. If the instrument channel port is able to be rotated or turned, do not use the endoscope and return it to Olympus for repair. If the instrument channel port does not rotate or turn, go to step 2. Step 2: Visually inspect the rubber part around the instrument channel port of the referenced endoscope. If the rubber part is in a normal condition as shown in picture 02, the endoscope can be used in a patient procedure. If the rubber part is lifted from the molding parts as shown in picture 03, do not use the endoscope and return it to Olympus for repair. If you have any questions about how to conduct this important inspection or you are not sure of the results of your inspection, you should contact the Olympus Technical Assistance Center (TAC), prior to using the device again. The phone number for TAC is 1-800-848-9024 option 1. To request service for your endoscope, contact Olympus at 1-800-848-9024, option 3. If you may have further distributed this product, please identify your customers and inform them at once of this action. Please complete and return the enclosed Reply Form to Olympus at facsimile (484) 896-7128.
- Quantity in commerce
- 3948
- Distribution
- The products were distributed US nationwide and Canada.
- Product codes and lots
- all lot codes
Enforcement reports
One row per recalled product line| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-3283-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3284-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3285-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3286-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3287-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3288-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3289-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3290-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3291-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3292-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3293-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3294-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3295-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3296-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3297-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3298-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3299-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3300-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3301-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3302-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3303-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3304-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3305-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3306-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3307-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3308-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3309-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3310-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3311-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-3312-2018 | Class II | Terminated | Voluntary: Firm initiated |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
