TIDI AquaGuard dressings recalled due to temperature excursions between June 1 and August 30, 2021. Product may have been less effective if stored at higher temperatures during shipping.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.
TIDI's AquaGuard dressings were recalled because they were exposed to higher temperatures between June 1 and August 30, 2021. This could have reduced their effectiveness but is unlikely to cause health problems.
The dressings were shipped with temperatures outside the recommended range from June 1 to August 30, 2021. This could have made the dressings less effective but does not pose a risk of injury or illness.
Healthcare facilities that received these dressings between June 1 and August 30, 2021. Staff using the dressings for wound care are most at risk if the product was stored improperly.
Check for the catalog numbers 68751510104 (7x7 dressings) or 68751510105 (10x12 dressings) purchased between June 1 and August 30, 2021.
Look for the catalog numbers 68751510104 or 68751510105 on the packaging.
No, the recall states that the dressings are unlikely to cause health problems due to temperature issues.
The recall covers dressings received between June 1 and August 30, 2021.
Check for catalog numbers 68751510104 (7x7 dressings) or 68751510105 (10x12 dressings) purchased between June 1 and August 30, 2021.
We’ve drafted a message you can send TIDI to request your refund or repair — edit it as you like.
Subject: Recall Z-1798-2022 — TIDI TIDI Hello, I own a TIDI that is covered by recall Z-1798-2022 from TIDI. 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.
