CLASS I Drug recall · Reported 20 Mar 2019 · FDA Enforcement Report

NET Remedies #3 Homeopathic Preparation, Oral Liquid recalled

King Bio is recalling NET Remedies #3 Homeopathic Preparation, Oral Liquid, Manufacturer: King Bio Inc. U.S.A, distributed nationwide in the US. The recall was initiated on 20 Jul 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLots: AUS-011117C Exp. 01/20; AUS-011916C Exp. 01/19; AUS-030816C Exp. 03/19; AUS-050516C Exp. 05/19; AUS-061217A Exp. 06/20; AUS-081516F Exp. 08/19; AUS-091515C Exp. 09/18

Quantity recalled2900 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-0919-2019
FDA event ID: 80601
Recalling firm: King Bio, Asheville, NC
Classification: Class I
Status: Terminated
Recall initiated: 20 Jul 2018
FDA classified: 8 Mar 2019
Reported: 20 Mar 2019
Type: Voluntary: Firm initiated
Customers notified by: Press Release
Reason category: Sterility

Timeline

20 Jul 2018	Recall initiated by company
8 Mar 2019	Classified by FDA	+231 days
20 Mar 2019	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Microbial contamination

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

NET Remedies #3 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia

Where it was distributed

U.S.A. Nationwide, Canada, and Australia.

Nationwide

Questions about this recall

Is NET Remedies #3 Homeopathic Preparation, Oral Liquid, Manufacturer: King Bio Inc. U.S.A recalled?

Yes. King Bio recalled NET Remedies #3 Homeopathic Preparation, Oral Liquid, Manufacturer: King Bio Inc. U.S.A on 20 Jul 2018. The recall is Class I and its status is Terminated. Recall number D-0919-2019.

Why was it recalled?

Microbial contamination

Which lots are affected?

Lots: AUS-011117C Exp. 01/20; AUS-011916C Exp. 01/19; AUS-030816C Exp. 03/19; AUS-050516C Exp. 05/19; AUS-061217A Exp. 06/20; AUS-081516F Exp. 08/19; AUS-091515C Exp. 09/18

Where was it sold?

U.S.A. Nationwide, Canada, and Australia.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from King Bio

All 465

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20 Mar 2019Drug	CLASS I	Dr. King's SafeCare Rx LymePlex, King Bio, Inc. recalled	King Bio	Sterility	Nationwide
20 Mar 2019Drug	CLASS I	Dr. King's SafeCare Rx CS-Lymph Hodgkins, King Bio, Inc. recalled	King Bio	Sterility	Nationwide
20 Mar 2019Drug	CLASS I	Dr. King's SafeCare Rx Smoke Control, King Bio, Inc. recalled	King Bio	Sterility	Nationwide
20 Mar 2019Drug	CLASS I	Dr. King's SafeCare Rx Gout Symptom Relief, King Bio, Inc. recalled	King Bio	Sterility	Nationwide
20 Mar 2019Drug	CLASS I	Dr. King's Natural Medicine Homeopathic Climate Adaptation recalled	King Bio	Sterility	Nationwide