Mckesson recalls LiquiBand Exceed adhesive products made between June and September 2021 due to potential temperature issues during shipping that might affect product effectiveness. No health risks reported.
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.
Mckesson is recalling specific LiquiBand Exceed adhesive products made between June and September 2021 because they may have been exposed to higher temperatures during shipping. This could affect how well the adhesive works but is unlikely to cause health problems.
The adhesive products were stored at temperatures outside the recommended range during shipping from June to August 2021. This might reduce their effectiveness but does not pose a health risk to users.
Healthcare workers using these adhesives for medical procedures are most likely affected. Patients receiving treatments with these products could also be impacted.
Check for model numbers 122-LBXS (0.4mL) or 122-LBX (0.8mL) on the packaging. Products with lot codes from June to September 2021 are included in this recall.
Look for model numbers 122-LBXS or 122-LBX on the packaging or product label.
No health risks are reported; the product may not work as intended but is unlikely to cause harm.
Products were made between June 1 and September 30, 2021.
Check for model numbers 122-LBXS (0.4mL) or 122-LBX (0.8mL) and lot codes from June to September 2021.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1788-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-1788-2022 from Mckesson Medical-Surgical. 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.
