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Serious recall: Injury is possible or has been reported. Take action promptly.

HTO Nevada, Inc. 2023-02-22 Health serious FDA
Health · FDA · Recall #FDA-D-0271-2023

Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure,… Recall

Issued February 22, 2023 · HTO Nevada, Inc.

In February 2023, HTO Nevada, Inc. recalled the Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure,…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.

What you should do

  1. 1 Stop using Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure,… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact HTO Nevada, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
HTO Nevada, Inc.
Category
Health
Recall date
February 22, 2023
Units affected
Not reported
Sold at
Nationwide in the USA and Canada.
Recall number
FDA-D-0271-2023
Made in
United States
Issuing agency
FDA

In context

  • HTO Nevada, Inc. has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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