Drugs & medicalClass II

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…

Read the official notice →
Date
2023-11-29
Country
United States
Brand
Aizu Olympus
Product
Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum and sigmoid colon).…
Classification
Class II
Units
Worldwide - US Nationwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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

  1. 2025-12-10
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    Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

    FDA · DeviceAizu Olympus Co., Ltd.US Nationwide distribution.Official notice →
  3. 2023-12-06
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    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 →
  5. 2022-08-31
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    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.

    FDA · DeviceAizu Olympus Co., Ltd.US Nationwide distribution in the states of FL, IL, NC, PA & TX.Official notice →
All 4 Aizu Olympus recalls →

Other drugs & medical recalls in the United States

  1. 2023-11-29
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    Due to an increased risk of degradation of the power entry switch resulting from arcing inside of the power switch that may result in carbon build-up on the switch contacts. The carbon build-up may lead to excess…

    FDA · DeviceBioFire Diagnostics, LLCWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
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    Roche Diagnostics Operations, Inc. recalls Tina-quant D-Dimer Test System, Fibrinogen/Fibrin Degradation Products Assay, Material Numbers 03001245322 - (cobas c 311,…

    Elevated results were detected with Li-heparin plasma samples when compared to citrated plasma samples.

    FDA · DeviceRoche Diagnostics Operations, Inc.US Nationwide distribution.Official notice →
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    Becton Dickinson & Company recalls BD gravity sets (Product Name, Catalog #) 32-IN GRAV SET W/0.2 MICRON FILTER BAG ACCESS PORT SS VALVE TEXIUMTM LOW ABSORPTION,…

    Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

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    Sentinel CH SpA recalls IRON assay, Reference Numbers 6K95-41 and 6K95-30

    A high recovery of Iron assay has been observed at some customer sites. Internal studies confirmed the positive shift of Quality Control and patient samples results, up to 15% for Iron Products (Alinity c Iron Reagent…

    FDA · DeviceSentinel CH SpAWorldwide - US Nationwide distribution.Official notice →
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    Convergent Dental recalls Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly SUB-00434 with foot pedal CUS-00226 Rev. K reworked

    It has been found that potential unintended laser activation can occur without foot pedal depression.

    FDA · DeviceConvergent DentalWorldwide - US Nationwide distribution in the states of AK, AL, CA, CT, FL,…Official notice →
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    Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous…

    Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.

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See all drugs & medical recalls →