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Unrated Drug recall · FDA · Published June 26, 2019

Riverpoint Pharmacy recalls PAP/PHEN/PGE1 injection due to lack of sterility assurance

Riverpoint Pharmacy recalls 5mL PAP/PHEN/PGE1 22 mg/0.8mg/8mcg/mL injection (Lot 06112019@32) due to lack of sterility assurance. This medication is prescription-only and may cause infection if used.

🇺🇸 FDA recall #D-1479-2019DrugRiverpoint Pharmacy ›
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Recalling firmFirst Pharma Associates LLC dba Riverpoint Pharmacy1802 N Monroe St · Spokane, WA 99205-4528
✎ GovInfoNow plain-language explainer

What happened, in plain English

Riverpoint Pharmacy is recalling a specific prescription injection product because it lacks assurance of sterility. Using this product could lead to infections if it's not properly sterilized. Read more at govinfonow.com/recall/38489-riverpoint-pharmacy-recalls-pap-phen-pge1-injection-due-to-lack.

Source Summary by GovInfoNow · govinfonow.com/recall/38489-riverpoint-pharmacy-recalls-pap-phen-pge1-injection-due-to-lack · Updated October 5, 2026 · FDA enforcement record: FDA #D-1479-2019

Cite this page

“Riverpoint Pharmacy recalls PAP/PHEN/PGE1 injection due to lack of sterility assurance.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38489-riverpoint-pharmacy-recalls-pap-phen-pge1-injection-due-to-lack. Based on FDA recall #D-1479-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1479-2019%22&limit=1).

Why it’s dangerous

The injection product lacks assurance of sterility, meaning it may not be clean enough to prevent infections. This is a serious risk for patients who use it without proper sterilization.

Who’s affected

Prescription patients who received this specific injection product from Riverpoint Pharmacy in Spokane, WA. Those with the Lot number 06112019@32 are most at risk.

How to tell if you have this one

Check for the product name 'PAP/PHEN/PGE1 22 mg/0.8mg/8mcg/mL Injection, 5mL vial' and the lot number 06112019@32. This medication is prescription-only and sold by Riverpoint Pharmacy in Spokane, WA.

  • Brand
    Riverpoint Pharmacy
  • Category
    Drug
FDA recall event · 18 products

All 18 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
    ID, WA only
Recall numberProduct, codes & lotsQuantity
D-1468-2019Testosterone Cypionate 100 mg/mL Sesame Oil Injection, 12mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 04192019@1, Exp. 07/21/2019; 05312019@4, Exp. 09/03/201924 mL
D-1469-2019Testosterone Cypionate 150 mg/mL Sesame Oil Injection, 12 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343- 6252.; Lot #: 04202019@1, Exp. 07/21/201912 mL
D-1470-2019Testosterone Cypionate 200 mg/mL Sesame Oil Injection, packaged in a) 9 mL, b) 12 mL vials, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343- 6252; Lot #: a) 05022019@31, Exp. 08/4/2019; 05152019@18, Exp. 08/13/2019; b) 05292019@4, Exp. 08/28/2019.a) 18 mL b) 12mL
D-1471-2019Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection, packaged in a) 7.2 mL. b) 9.6 mL, c) 10.8mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.; Lot #: a) 05032019@18, Exp. 08/04/2019; b) 05062019@20, Exp. 08/06/2019; c) 05132019@1, Exp. 08/13/2019.a) 14.4 mL, b) 9.6 mL, c) 10.8 mL
D-1472-2019Testosterone Cypionate 100 mg/mLOil Injection Injection, 12 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.; Lot #: 05152019@36, Exp. 09/09/201912 mL
D-1473-2019Testosterone Cyp/Estradiol Cyp 50 mg/2.5 mg/mL Injection, 3mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.; Lot #: 06102019@31, Exp. 09/09/20193 mL
D-1474-2019Hydroxyprogesterone Caproate 250 mg/mL Sesame Oil Injection, 5 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 05152019@17, Exp. 08/13/201950 mL
D-1475-2019Prostaglandin 20 mcg/mL/Procaine 0.1% Injection, packaged in a) 2.5mL and b)10 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205 (509) 343-6252; Lot #: a) 06182019@16, Exp. 08/04/2019 b) 06032019@8, Exp. 07/18/2019a) 2.5 mL b) 10 mL
D-1476-2019Hydroxocobalamin 10 mg/mL Injection (ALT) Solution, 30 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 05282019@53, Exp. 08/26/2019 and Exp. 08/28/201960 mL
D-1477-2019Methylcobalamin 1 mg/mL Injection, 8 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06102019@6, Exp. 08/09/20198 mL
D-1478-2019Methylcobalamin 10 mg/mL Injection, 5.4 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.; Lot #: 06202019@29, Exp. 08/19/20195.4 mL
D-1479-2019PAP/PHEN/PGE1 22 mg/0.8mg/8mcg/mL Injection, 5mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06112019@32, Exp. 07/27/20195 mL
D-1480-2019PAP/PHEN/PGE1 30 mg/2mg/20mcg/mL Injection, 10mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06122019@16, Exp. 07/27/201910 mL
D-1481-2019PAP/PHEN/PGE1 30 mg/0.83mg/10mcg/mL Injection, 5 mL, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06122019@9, Exp. 07/28/20195 mL
D-1482-2019PAP/PHEN/PGE1 18 mg/0.6mg/5.88mcg/mL Injection, 5 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06152019@1, Exp. 08/2/20195 mL
D-1483-2019Chorionic Gonadotropin 2,000U/mL PF Injection, 8 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06212019@15, Exp. 07/24/20198 mL
D-1484-2019Glutathione 100 mg/mL Inhalation Solution (PF), 45 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252; Lot #: 06172019@3, Exp. 08/18/201945 mL
D-1485-2019Serum Tears 20% Eye Drops PF Solution, packaged in a) 15 EA, b)15 mL vials, c) 12 EA, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343- 6252; Lot #: a) 06042019@20, Exp. 07/19/2019; 06052019@24, Exp. 07/28/2019; 06062019@10, Exp. 07/21/2019; b) 06132019@6, Exp. 07/29/2019; c) 06182019@28, Exp. 12/17/2019, 06192019@28, Exp. 12/18/2019.a) 60 EA, b) 15mL, c) 24 EA
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name and lot number 06112019@32 on the vial.

Where it went and when

Where it was distributed

Distributed in Idaho and Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: 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: not listedNCSouth 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: “ID, WA only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Idaho, Washington.

Recall timeline

FDA terminated this recall 3.9 years after the firm started it.

1. Firm started the recall: Jun 26, 201912. FDA classified it Class II: Jul 11, 201923. Published in FDA’s Enforcement Report: Jul 17, 201934. FDA terminated the recall: Jun 6, 2023420192023
  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-1479-2019 (June 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1479-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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