Shanghai United Imaging Healthcare Co., Ltd. recalls uEXPLORER PET/CT System - Product Usage: intended to be operated by qualified healthcare professionals to assist in…
The EXAM acquisition workflow could occasionally freeze after canceling the PET scan.
Read the official notice →- Date
- 2021-10-06
- Country
- United States
- Brand
- Shanghai United Imaging Healthcare
- Product
- uEXPLORER PET/CT System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detection,…
- Classification
- Class II
- Units
- U.S. Nationwide distribution in the states of CA, IL, IN, TX, and WI.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Shanghai United Imaging Healthcare recalls
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Other drugs & medical recalls in the United States
- 2021-10-06
- US
Beckman Coulter Inc. recalls DxA 5000 (DxA Automation System, DxA 5000 fit), "For in Vitro Diagnostic Use", Reference Numbers: B87352 with B57634, UDI: 15099590707118
There is a potential that sample carriers (w or w/o samples) within automated sampling system may transport samples to the outer lane which does not contain a physical barrier to restrain samples. Samples are dropped…
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Hill-Rom, Inc. recalls LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC, Wide Model Number: 3156065B (obsolete since 12JUN2020) - The…
Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may…
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GE Healthcare, LLC recalls Flow sensors that may be installed in the following GEHC anesthesia machines: (1) Aestiva MRI, GTIN 0080682102339; (2) Aestiva 7900; (3)…
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Atrium Medical Corporation recalls Atrium Pneumostat Chest Drain Valve, Part Number 16100
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Elekta, Inc. recalls MOSAIQ Oncology Information System
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