Aizu Olympus Co., Ltd. recalls EVIS EXERA III Bronchovideoscope
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
Read the official notice →- Date
- 2022-08-31
- Country
- United States
- Brand
- Aizu Olympus
- Product
- EVIS EXERA III Bronchovideoscope
- Classification
- Class II
- Units
- US Nationwide distribution in the states of FL, IL, NC, PA & TX.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Aizu Olympus recalls
- 2025-12-10
USAizu Olympus Co., Ltd. recalls Olympus OER-Elite
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- 2023-12-06
- US
Aizu Olympus Co., Ltd. recalls PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or…
FDA · DeviceAizu Olympus Co., Ltd.Domestic distribution to FL, KY, MA, NJ, NY, and PAOfficial notice → - 2023-11-29
- US
Aizu Olympus Co., Ltd. recalls Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum and sigmoid colon).…
Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for…
Other drugs & medical recalls in the United States
- 2022-08-31
- US
DeRoyal Industries Inc recalls DeRoyal limb holders: (1) DeRoyal Limb Holder, Wrist, Fixed, Quick Release, REF M8124; (2) DeRoyal Limb Holder, Ankle, Fixed, Quick…
The webbing strap was laced improperly through the teeth of the buckle allowing the webbing strap to slide and was, therefore, not secure.
FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the states of FL, IN, NV, RI, TN, TX, and WV.Official notice → - US
Synapse Biomedical Inc recalls NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.
Due to a defect identified on the EPG controller printed circuit board assembly, device performance may degrade over time. Depending on the failure mode, potential adverse events include pain, muscle fatigue and…
FDA · DeviceSynapse Biomedical Incdistribution to US states of AL, CO, IL, FL, GA, MD, MN, NC, NJ, OH, PA, and…Official notice → - US
Getinge Usa Sales Inc recalls Maquet Critical Care AB/Getinge Servo-u Ventilator System, Part Number 6694800 Servo-n Ventilator System, Part Number 6688600 Servo-u MR…
Ventilators may generate a combination of alarms which may result in loss of communication, technical alarms being triggered, and loss of ventilation. If the device stops ventilating due to this issue, it may lead to…
FDA · DeviceGetinge Usa Sales IncWorldwide distribution. US nationwide, Poland, Spain, France, Germany, Czech…Official notice → - US
Hamilton Medical AG recalls HAMILTON-C6 Intensive Care Ventilator, REF: 160021
Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety…
- US
Intera Oncology, Inc. recalls INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
Higher than expected flow rate.
FDA · DeviceIntera Oncology, Inc.US distribution to states of: AL, CA, IL, KY, MN, MO, NC, NJ, NY, OH, OR, PA,…Official notice → - US
Midlab Incorporated recalls Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern…
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.