Galt Medical recalls TVS LPA devices with catalog # DIL-059-00 due to potential bacterial endotoxins causing fever, chills, and hypotension. Affected units include specific lot numbers.
The products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bacteria can activate the inflammatory process and produce fever, chills, and hypotension in a patient.
Galt Medical is recalling TVS LPA devices that may contain unsafe levels of bacterial endotoxins. This can cause fever, chills, and low blood pressure in patients. The recall affects specific lot numbers of the product.
Bacterial endotoxins (pyrogens) can trigger an inflammatory response in the body, leading to fever, chills, and low blood pressure. These effects are more severe in individuals with weakened immune systems.
Patients using the TVS LPA device are most at risk, particularly those with compromised immune systems. The recall applies to specific lot numbers of the device.
Check the catalog number DIL-059-00 on the device. Affected units include lot numbers 17338821 and 18019045.
Look for the lot number on the device packaging or label to confirm if it is affected (17338821 or 18019045).
The device may contain bacterial endotoxins that can cause fever, chills, and low blood pressure in patients.
Check the catalog number DIL-059-00 and lot numbers 17338821 or 18019045 on the device packaging.
The recall does not require immediate discontinuation; check the lot number to determine if your device is affected.
We’ve drafted a message you can send Galt Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2564-2018 — Galt Medical Galt Medical Hello, I own a Galt Medical that is covered by recall Z-2564-2018 from Galt Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
