SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION recalls Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems…
Due to an issue (potential breakage) with the shaft for the mounting of the X-ray tube assembly that could potentially result assembly coming off the rotating shaft.
Read the official notice →- Date
- 2025-11-19
- Country
- United States
- Brand
- Shimadzu Corporation Medical Systems Division
- Product
- Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The ceiling type x-ray…
- Classification
- Class II
- Units
- Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Shimadzu Corporation Medical Systems Division recalls
- 2024-11-13
USSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION recalls SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic…
X-ray R/F system software with certain versions of the control board may occasionally fail to display images when switching from Fluoroscopy mode to Radiography mode, which may lead to the possibility of delay or…
FDA · DeviceSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISIONUS Nationwide distribution in the states of CA, CT, MA, WV, OH, NY, IA, NE,…Official notice →- 2024-10-30
- US
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION recalls Trinias unity, Digital Angiography System with Catheterization Table, Model: KS-100 This system consists of the…
If digital angiography system is used with a specific catheterization table and the operator directs simultaneous movement of the table and the C-arm using direct memory, then direct memory button is released, the…
FDA · DeviceSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISIONUS Nationwide distribution in the states of MA, IL, SC, KY, SC, OH, TN.Official notice → - 2024-03-20
- US
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION recalls Shimadzu, Trinias, Digital Angiography System
Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
FDA · DeviceSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISIONUS Nationwide distribution in the states of OH.Official notice → - 2023-08-09
- US
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION recalls Over-Head Ceiling Tube Support, CH-200, CH-200M, Used with RadSpeed and RadSpeed PRO, Sonial Vision safire, Versa…
Eight fixing bolts at the base of the X-ray ceiling tube column assembly may be loose or missing so service is required to install a cable, bracket, and label behind the bracket, indicating when service is required, to…
FDA · DeviceSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISIONU.S. Nationwide distribution.Official notice →
Other drugs & medical recalls in the United States
- 2025-11-26
- US
Alembic Pharmaceuticals Limited recalls Fesoterodine Fumarate, Extended-release Tablets, 4 mg, 30-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals…
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
- 2025-11-19
- US
TECHNO-PATH MANUFACTURING LTD. recalls Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control serum to…
Potential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform.
FDA · DeviceTECHNO-PATH MANUFACTURING LTD.US distribution to CA, CO, CT, FL, HI, IL, LA, MI, MN, NV, NY, OR, SC, TN, TX,…Official notice → - US
Accriva Diagnostics, Inc. recalls VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in…
Due to an device without a premarket clearance being incorrectly package and distributed.
FDA · DeviceAccriva Diagnostics, Inc.Worldwide - U.S. Nationwide distribution in the states of AK, CA, FL, IA, IL,…Official notice → - US
Applied Medical Technology Inc recalls Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
The nasal feeding tube may be occluded
FDA · DeviceApplied Medical Technology IncUS Nationwide distribution in the states of MA, RI, NC, OH.Official notice → - US
Siemens Healthcare Diagnostics, Inc. recalls Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4;
The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode…
FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide - US Nationwide distribution in the state of CA and the countries of…Official notice → - US
Stryker Sustainability Solutions recalls HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.
FDA · DeviceStryker Sustainability SolutionsUS Nationwide distribution and OUS (foreign) to country of: Canada.Official notice →