Mckesson Medical-Surgical recalls Triamcinolone Acetonide cream 0.1% 15g tubes due to temperature abuse risks. This prescription-only product may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Triamcinolone Acetonide cream (0.1% 15g tubes) because of temperature abuse risks. This prescription-only product could be unsafe if stored or handled at improper temperatures.
The cream may be affected by temperature abuse, meaning improper storage or handling could lead to unsafe conditions. This is a regulatory issue related to manufacturing quality control.
Prescription patients who received this specific cream from a pharmacy. Those with the product may be at risk if it was exposed to temperatures outside the recommended range.
Check for the product name 'Triamcinolone Acetonide cream, USP, 0.1%, 15 grams tube, Rx only' with manufacturer Sandoz Pharma and NDC 0168-0004-15. The recall covers specific lots distributed to customers.
Identify the product by checking the label for 'Triamcinolone Acetonide cream, USP, 0.1%, 15 grams tube, Rx only' with manufacturer Sandoz Pharma and NDC 0168-0004-15.
The recall indicates potential temperature abuse risks, but the official notice does not specify if the product is safe to use without proper temperature control.
The recall states that McKesson Medical-Surgical cannot identify the specific lot number for each consignee, so lot numbers cannot be determined from this notice.
The official recall notice does not provide specific action steps for consumers, only that the product may be affected by temperature abuse.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1106-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1106-2022 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.
