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Stop using now Drug recall · FDA · Published August 6, 2020

Family Pharmacy Recalls Lorazepam Infusion Due to Sterility Risk

Family Pharmacy of Statesville recalls Lot 07312020@6 Lorazepam 1 mg/mL bags due to lack of sterility assurance. Check your prescription.

🇺🇸 FDA recall #D-0665-2022DrugFamily Pharmacy of Statesville ›
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Recalling firmFamily Pharmacy of Statesville3478 E Broad St · Statesville, NC 28625-4523
✎ GovInfoNow plain-language explainer

What happened, in plain English

Family Pharmacy of Statesville is recalling one bag of Lorazepam 1 mg/mL Infusion Solution because it lacks assurance of sterility. The affected item is Lot #07312020@6 with a Beyond Use Date (BUD) of 8/7/2020. This recall was issued on August 6, 2020, and the product was distributed only in North Carolina. Read more at govinfonow.com/recall/36851-family-pharmacy-recalls-lorazepam-infusion-due-to-sterility-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/36851-family-pharmacy-recalls-lorazepam-infusion-due-to-sterility-risk · Updated October 11, 2026 · FDA enforcement record: FDA #D-0665-2022

Cite this page

“Family Pharmacy Recalls Lorazepam Infusion Due to Sterility Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/36851-family-pharmacy-recalls-lorazepam-infusion-due-to-sterility-risk. Based on FDA recall #D-0665-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0665-2022%22&limit=1).

Why it’s dangerous

The product lacks assurance of sterility, meaning it may contain harmful microorganisms. Administering a non-sterile infusion solution can lead to serious infections or other complications in patients.

Who’s affected

Patients in North Carolina who received Lorazepam infusion solution from Family Pharmacy of Statesville between the manufacturing date and the recall date. Individuals with this specific lot number are at risk of infection due to potential non-sterility.

How to tell if you have this one

Check your prescription for Lorazepam 1 mg/mL Infusion Solution in 250 mL bags. Look specifically for Lot #07312020@6 and a Beyond Use Date (BUD) of 8/7/2020. The product was sold by Family Pharmacy of Statesville.

  • Brand
    Family Pharmacy of Statesville
  • 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
    NC only
Recall numberProduct, codes & lotsQuantity
D-0656-2022Hydromorphone HCl 2 mg/mL Infusion 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07212020@4 BUD: 10/19/2020; 07212020@4 BUD: 10/30/20202 bags
D-0657-2022Hydromorphone HCl 1 mg/mL 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07272020@2 BUD: 10/25/2020; 07302020@1 BUD: 10/28/2020; 08012020@1 BUD: 10/30/20204 bags
D-0658-2022Hydromorphone HCl 5 mg/mL Infusion in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07292020@7 BUD: 8/12/20201 bag
D-0659-2022Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 08022020@1 BUD: 8/17/20201 bag
D-0660-2022Trimix (Alprostadil/Papaverine/Phentolamine) 20 mcg/30 mg/0.5 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07212020@ BUD: 9/4/20202 vials
D-0661-2022Trimix (Alprostadil/Papaverine/Phentolamine) 10 mcg/20 mg/1 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.; Lot #:07232020@1 BUD: 9/6/2020; 07282020@1 BUD: 9/11/2020; 07282020@2 BUD: 9/11/20205 vials
D-0662-2022Vancomycin14 mg/mL Fortified Ophthalmic Solution in 5 mL bottles, Rx only, Family Pharmacy of Statesville, Inc.; Lot: 07312020@2 BUD: 9/14/20203 bottles
D-0663-2022Morphine Sulfate 6 mg/mL Infusion in 250 mL bag, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07212020@3 BUD: 10/19/2020; 07292020@2 BUD: 10/27/20208 bags
D-0664-2022Ketamine 50 mg Infusion (LV 1) Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07212020@1 BUD: 8/4/2020; 07232020@2 BUD: 8/6/2020; 07302020@2 BUD: 8/13/20203 bags
D-0665-2022Lorazepam 1 mg/mL Infusion Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07312020@6 BUD: 8/7/20201 bag
D-0666-2022Methylcobalamin 1 mg/mL Injectable in 1 mL syringes, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07282020@3 BUD: 8/11/20205 syringes
D-0667-2022Fentanyl 150 mcg/mL Infusion Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.; Lot #: 07312020@5 BUD: 8/14/20201 bag
Based on the official FDA remedy

What to do — step by step

  1. Stop using the medication

    Do not use the Lorazepam infusion solution if it matches the recalled lot number and BUD.

  2. Contact your pharmacy

    Reach out to Family Pharmacy of Statesville for instructions on returning or disposing of the product.

Where it went and when

Where it was distributed

Distributed in North Carolina.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: North Carolina.

Recall timeline

FDA terminated this recall 3 years after the firm started it.

1. Firm started the recall: Aug 6, 202012. FDA classified it Class II: Mar 17, 202223. Published in FDA’s Enforcement Report: Mar 23, 202234. FDA terminated the recall: Aug 15, 2023420202023
  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-0665-2022 (August 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0665-2022 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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