Drugs & medicalClass II

Karl Storz Endoscopy recalls Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF: 26153EAU/1.

Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact the assurance of sterility.

Read the official notice →
Date
2026-07-29
Country
United States
Brand
Karl Storz Endoscopy
Product
Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF: 26153EAU/1.
Classification
Class II
Units
US Nationwide distribution in the states of FL, MA, MN, TX, OH, NY, CA, MI,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Karl Storz Endoscopy recalls

  1. 2026-10-07
  2. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for…

    Due to incorrect inside packaging label for eyepiece.

    FDA · DeviceKarl Storz EndoscopyU.S. Nationwide distribution in the states of AZ, CA and MO.Official notice →
  3. 2025-02-05
  4. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls KARL STORZ - ENDOSKOPE, REF: 27010L, Uretero-Renoscope, 7 Fr., 43cm, NON STERILE, RxONLY, CE 0123

    Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

    FDA · DeviceKarl Storz EndoscopyUS Nationwide distribution.Official notice →
  5. 2025-01-22
  6. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE

    Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.

    FDA · DeviceKarl Storz EndoscopyUS: AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN,…Official notice →
  7. 2024-12-04
  8. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls 4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5 x 120 mm REF…

    Due to holes detected in the inner barrier system that may compromise the sterility of the affected products.

    FDA · DeviceKarl Storz EndoscopyWorldwide - U.S. Nationwide distribution in the states of AL, FL, IA, IN, KS,…Official notice →
  9. 2024-11-20
  10. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC

    Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S.

    FDA · DeviceKarl Storz EndoscopyU.S. Nationwide distribution in the states of CO, CT, DC, MD, MI, MN, NC, NY,…Official notice →
  11. 2024-10-02
  12. US
    Drugs & medicalClass II

    Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123

    Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

    FDA · DeviceKarl Storz EndoscopyUS Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT,…Official notice →
All 17 Karl Storz Endoscopy recalls →

Other drugs & medical recalls in the United States

  1. 2026-08-05
  2. US
  3. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Azelaic Acid Gel, 15%, 50 gram tubes, For Topical Use only, Rx only, Distributed by: Glenmark Pharmaceuticals Inc., USA,…

    CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.

    FDA · DrugGlenmark Pharmaceuticals Inc., USANationwide within the United States.Official notice →
  4. US
    Drugs & medicalClass II

    MICRO LABS USA INC recalls Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India,…

    Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.

    FDA · DrugMICRO LABS USA INCNationwide in the USA.Official notice →
  5. 2026-07-29
  6. US
    Drugs & medicalClass II

    Alphatec Spine, Inc. recalls SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System

    Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication…

    FDA · DeviceAlphatec Spine, Inc.US Nationwide distribution in the states of TX, MO, IN.Official notice →
  7. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline medical convenience kits labeled as: 1) SHOULDER PACK, Medline Kit SKU DYNJ39590O; 2) SHOULDER PACK, Medline Kit SKU DYNJ88566; 3)…

    Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.

    FDA · DeviceMedline Industries, LPUS: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.Official notice →
  8. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. ROBOTIC CDS980523M

    Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of…

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of CA, FL, MD. PA, and TX.Official notice →
See all drugs & medical recalls →