Shimadzu Corp. Analytical & Measuring Instruments Div. recalls Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
There have been cases of failure of the main board due to condensation water drained from the Peltier dehumidifier, leaked out from the tray, resulting in a short circuit. In the serious case, the main board and…
Read the official notice →- Date
- 2024-12-04
- Country
- United States
- Brand
- Shimadzu Corp. Analytical & Measuring Instruments Div
- Product
- Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of MS, AR, TX, CA, MA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Corp. Analytical & Measuring Instruments Div recalls
- 2024-12-04
USShimadzu Corp. Analytical & Measuring Instruments Div. recalls Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
There have been cases of failure of the main board due to condensation water occurring in the gap between thermal insulation material on the underside of the main base dropping onto the main board The symptoms and…
FDA · DeviceShimadzu Corp. Analytical & Measuring Instruments Div.Worldwide - US Nationwide distribution in the states of DE, PA and the country…Official notice →
Other drugs & medical recalls in the United States
- 2024-12-04
- US
MEDLINE INDUSTRIES, LP - Northfield recalls ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use…
Identified lots of Olympus product may be missing sterile and manufacturing lot numbers and expiration dates on the sterile packaging. The information can be found on the outer box or zipper bag label. Medline is…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of NY.Official notice → - US
Remote Diagnostic Technologies Ltd. recalls Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or…
Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.
FDA · DeviceRemote Diagnostic Technologies Ltd.U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.Official notice → - US
Shimadzu Corp. Analytical & Measuring Instruments Div. recalls Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
There have been cases of failure of the main board due to condensation water occurring in the gap between thermal insulation material on the underside of the main base dropping onto the main board The symptoms and…
FDA · DeviceShimadzu Corp. Analytical & Measuring Instruments Div.Worldwide - US Nationwide distribution in the states of DE, PA and the country…Official notice → - US
Abbott Medical recalls Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted…
Due to heart transmitter not being able to upgrade to the current software version in the field after experiencing a power interruption during a prior over-the-wire software download.
FDA · DeviceAbbott MedicalWorldwide - U.S. Nationwide distribution in the states of ALABAMA, ALASKA,…Official notice → - US
GE Healthcare (China) Co., Ltd. recalls GE Proteus XR/A radiographic system
Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the Preventative Maintenance Action List.
- US
INCIPIO DEVICES recalls Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.
Recalled lot does not meet specification and has reported incidents of fracture of the TIG weld.