McGuff Compounding Pharmacy Services, Inc.

FDA recalling firm · 3 enforcement events · 4 product records · 2019–2022 · CA

McGuff Compounding Pharmacy Services, Inc. has 3 FDA enforcement events on this register (4 product records) between 2019 and 2022: 3 drug; the busiest year was 2019 with 2.

0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
8 Dec 2022	Thiamine Hydrochloride 200 mg/2mL (100mg/mL), Riboflavin 2 mg/2mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 2 mL Sterile Single Use Vial, Preservative-Free, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Services, Inc, Santa Ana, CA 92704.	Drug	Class II	2	Terminated
14 Feb 2019	Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding Pharmacy Services, Inc. Santa Ana, CA 92704	Drug	Class II	1	Terminated
10 Jan 2019	Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid), 1,200 mg/30 mL (40 mg/mL) Sterile 30 mL Multiple Dose Vial, Rx Only, McGuff Compounding Pharmacy Services, Inc., Santa Ana, CA 92704	Drug	Class II	1	Terminated

By type and class

Drug3

Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for McGuff Compounding Pharmacy Services, Inc. by year initiated.

Questions and answers

How many FDA recalls has McGuff Compounding Pharmacy Services, Inc. had?

3 enforcement events (4 product records) on this register, 2019–2022: 3 drug.

Are any McGuff Compounding Pharmacy Services, Inc. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are McGuff Compounding Pharmacy Services, Inc. recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.