9200C and 9200D Laryngeal Strobe Product Usage: The recall
9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of…
Why was 9200C and 9200D Laryngeal Strobe Product Usage: The recalled?
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
40552 22679-05 23546-06 23546-07 24036-06 24045-03 24045-06 24045-08 24045-09 24049-01 24049-03 24049-08 24231-10 24556-01 24556-06 24965-07 25282-03 25351-06 25459-01 25459-07 25459-08 25459-09 25461-01 25461-03 25461-05 25461-07 25461-09 25466-07 25466-08 25964-01 25964-03 25964-11 25965-02 25965-05 25965-12 26035-13 26055-02 26055-13 26055-18 26056-04 26056-05 26056-08 26057-03 26057-18 26058-18 26058-20 26870-09 26871-02 26871-02 26871-03 26871-03 26871-07 26871-11 26871-12 26871-14 26871-17 26871-18 26872-05 26872-06 26872-08 26872-10 26872-16 26872-18 26872-18 26872-20 26873-10 26873-16 26873-20 28073-02 28668-11 28670-03 28670-07 28670-12 28670-14 28672-14 28672-18 28674-03 28674-17 28676-08 29880-09 30001-02 30598-04 30598-09 30598-21 30599-04 30599-06 30599-13 30600-02 30600-03 30600-06 30601-11 30601-14 31523-07 31523-15 31523-21 31524-01 33226 33226-05 33226-06 33226-16 33413-05 33413-10 34162-07 34162-09 34162-20 34593-07 35263-06 35263-10 36135-14 36315-02 36315-13 36315-19 36600-13 36890-11 36890-12 36890-19 37419-13 37835-15 38524-09 38776-05 38850-01 38850-04 38850-06 39951-05 39952-024 39952-03 39952-04 41241-10 41577-09 41577-19 41577-20 41577-21 41861-14 41861-15 41861-16 42024-08 441046-01 45770-03 94965-03 48029-01 48029-06
- Product
- 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of…
- Recalling firm
- Pentax of America Inc
- Quantity
- 241 units in total
- Distribution
- Worldwide Distribution - US Nationwide
- Recall date
- July 26, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)