Reported Mar 6, 2024 · Ongoing
Colonoscope, Model Number CF-HQ190L.
Olympus Corporation of the Americas
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Olympus Corporation of the Americas · 3500 Corporate Pkwy · Center Valley, PA · 18034-8229
Is this the product you have?
- Colonoscope, Model Number CF-HQ190L.
- Lot codes and dates
- Model NumberCF-HQ190L
- UDI DI04953170305115
- Serial Number
97 of 97 codes
208272420828962082936208346120837652084560208505021862612187110218727421878112188037218820622005302201625220167722018442202345228848322889402289129228939122894212289572229097822914722303312230402423040702314598231539023917502391772239185723922812417328241745024177022417736241775524182022418754241884324190062419007241910525104892510795251080125111642512292251245825124702512569251281725132852524619252491626251442635605
- Amount recalled
- 97
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
Why it was recalled
Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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