Back Relief Ii (acetaminophen recalls

The FDA has published 1 recall involving Back Relief Ii (acetaminophen since 2022. The latest was reported on 16 Feb 2022. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2022

Last 12 months0reported

Class I00% of total

Ongoing0latest 16 Feb 2022

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why back relief ii (acetaminophen is recalled

Manufacturing (CGMP) Deviations1100%

Companies

ULTRAtab Laboratories1100%

By year

20221100%

All back relief ii (acetaminophen recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
16 Feb 2022Drug	CLASS II	Back Relief II (Acetaminophen 200 mg recalled by ULTRAtab Laboratories	ULTRAtab Laboratories	Manufacturing (CGMP) Deviations	NY

Should you stop taking Back Relief Ii (acetaminophen?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.