Pivotal Health Solutions, Inc. recalls Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable target…
This product is being recalled due to potentially insufficient rework on a part (E7130-B) on the lumbar section of the frame on 6 distributed tables. There were 4 additional tables with the faulty E7130-B part that…
Read the official notice →- Date
- 2024-07-17
- Country
- United States
- Brand
- Pivotal Health Solutions
- Product
- Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable target treatment…
- Classification
- Class II
- Units
- Distributed to CA, FL, TX, ID, GA, and TN
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Pivotal Health Solutions recalls
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FDA · DevicePivotal Health Solutions, Inc.Distribution to US nationwide, Canada and Japan.Official notice →
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