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  4. CPG Sec 585.500 Mushrooms, Canned or Dried (Freeze-Dried or Dehydrated) - Adulteration Involving Maggots, Mites, Decomposition
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COMPLIANCE POLICY GUIDE (CPG)

CPG Sec 585.500 Mushrooms, Canned or Dried (Freeze-Dried or Dehydrated) - Adulteration Involving Maggots, Mites, Decomposition November 2005

Final
Issued by:
Guidance Issuing Office
Office of Inspections and Investigations
Human Foods Program

REGULATORY ACTION GUIDANCE:

The following represents the criteria for recommending legal action to the CFSAN/Office of *Compliance*/Division of Enforcement (HFS-605):

Analyze for maggots or mites by AOAC 44.115-44.116, 14th edition or subsequent current revision. Analyze for decomposition by Macronalytical Procedures Manual V-100. Actionable if examination of minimum of six 100 g portions of drained canned mushrooms and proportionate amounts of liquid (contents of each can analyzed separately), or a minimum of six 15 g portions of dried mushrooms, from one code in lot shows one or more of the following:

  1. Maggots -- An average of 20 or more maggots of any size per 100 g of drained mushrooms and the proportionate liquid, or an average of 20 or more maggots of any size per 15 g of dried mushrooms;

    or

    An average of 5 or more maggots that are 2 mm or longer per 100 g portion of drained mushrooms and the proportionate liquid, or an average of 5 or more maggots that are 2 mm or longer per 15 g of dried mushrooms.
  2. or

  3. Mites -- An average of 75 or more mites per 100 g of drained mushrooms and the proportionate liquid, or an average of 75 or more mites per 15 g of dried mushrooms.
  4. or

  5. Decomposition -- An average of 10%; or more decomposed mushrooms by weight.

*Material between asterisks is new or revised*

Issued: 11/21/79

Reissued: 10/1/80

Revised: 12/8/88, 3/95, 5/2005

Updated: 11/29/05


Submit Comments

Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
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Rockville, MD 20852

All comments should be identified with the title of the guidance.

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