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Lower risk Drug recall · FDA · Published August 21, 2018

Auro Pharmacies Methyl-Cobalamin Injectables Recall: Sterility Risk

Auro Pharmacies recalls methyl-cobalamin injectables (5mL and 30mL vials) due to lack of sterility assurance. Products may cause infection if used improperly.

🇺🇸 FDA recall #D-1160-2018DrugAuro Pharmacies ›
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Recalling firmAuro Pharmacies, Inc.520 W La Habra Blvd · La Habra, CA 90631-5308
✎ GovInfoNow plain-language explainer

What happened, in plain English

Auro Pharmacies is recalling methyl-cobalamin injectable products because their manufacturing processes didn't properly ensure sterility. This could lead to infections if the products are used. Read more at govinfonow.com/recall/39694-auro-pharmacies-methyl-cobalamin-injectables-recall-sterility-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/39694-auro-pharmacies-methyl-cobalamin-injectables-recall-sterility-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-1160-2018

Cite this page

“Auro Pharmacies Methyl-Cobalamin Injectables Recall: Sterility Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39694-auro-pharmacies-methyl-cobalamin-injectables-recall-sterility-risk. Based on FDA recall #D-1160-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1160-2018%22&limit=1).

Why it’s dangerous

The products were made without proper sterility checks, meaning they could contain harmful bacteria. If injected, this could cause infections or other health issues.

Who’s affected

Prescription drug users who received the specific vial sizes and lot numbers from Auro Pharmacies' compounding pharmacy in La Habra, California. Healthcare providers and patients using these injectables are most at risk.

How to tell if you have this one

Check for vials labeled 'Methyl-Cobalamin injectable, 1 mg/mL' in 5mL or 30mL sizes. The lot number is 180618/2 with an expiration date of September 16, 2018.

  • Brand
    Auro Pharmacies
  • Category
    Drug
FDA recall event · 12 products

All 12 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide in USA
Recall numberProduct, codes & lotsQuantity
D-1156-2018CoEnzyme-Q10 injectable, 20 mg/mL, 10 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180626/3, Exp 25-Aug-1839 vials
D-1157-2018Calcium Gluconate injectable, 10%, 50 ml Single Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180626/10, Exp 24-Sep-18167 vials
D-1158-2018Dexpanthenol injectable, 250 mg/mL, 10 mL Single Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180529/2, Exp 27-Aug-18 and 180620/11, Exp 18-Sep-1891 vials
D-1159-2018Glutathione injectable, 200 mg/mL, 30 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180716/21, Exp 14-Oct-18183 vials
D-1160-2018Methyl-Cobalamin injectable, 1 mg/mL, packaged in a) 5 mL and b) 30 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: a) 180618/2, Exp 16-Sep-18; b) 180618/2, Exp 16-Sep-18114 vials
D-1161-2018Methyl-Cobalamin injectable, 5 mg/mL, 30 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180618/3, Exp 16-Sep-1890 vials
D-1162-2018Methyl-Cobalamin injectable, 10 mg/mL, 30 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180702/1, Exp 30-Sep-1881 vials
D-1163-2018Testosterone Cypionate/Enanthate injectable, 126/54 mg/mL, packaged in a) 3 mL and b) 5 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180709/21, Exp 07-Sep-1843 vials
D-1164-2018Testosterone Cypionate/Enanthate injectable, 200/50 mg/mL, packaged in a) 5 mL and 8 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180606/18, Exp 30-Nov-1832 vials
D-1165-2018Testosterone Enanthate/Cypionate injectable, 126/54 mg/mL, packaged in a) 3 mL and b) 5 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180709/24, Exp 07-Sep-1811 vials
D-1166-2018Folic Acid injectable, 10 mg/ml, 30 ml Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180611/1, Exp 09-Sep-1840 vials
D-1167-2018Methyl-Cobalamin injectable, 2 mg/mL, 30 ml Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631; Lot #: 180620/2, Exp 18-Sep-1874 vials
Based on the official FDA remedy

What to do — step by step

  1. Check Vial Details

    Look for vials with the lot number 180618/2 and expiration date September 16, 2018.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 17 months after the firm started it.

1. Firm started the recall: Aug 21, 201812. FDA classified it Class II: Aug 29, 201823. Published in FDA’s Enforcement Report: Sep 5, 201834. FDA terminated the recall: Jan 30, 2020420182020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-1160-2018 (August 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1160-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA