CLASS I Drug recall · Reported 26 Aug 2020 · FDA Enforcement Report
Desmopressin Acetate Nasal Spray 10 mcg/ glass vial with spray cap recalled
Ferring Pharmaceuticals is recalling Desmopressin Acetate Nasal Spray 10 mcg/ glass vial with spray cap, distributed nationwide in the US. The recall was initiated on 21 Jul 2020 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1505-2020
- FDA event ID
- 86066
- Recalling firm
- Ferring Pharmaceuticals, Parsippany, NJ
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Jul 2020
- FDA classified
- 17 Aug 2020
- Reported
- 26 Aug 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Potency & Assay
- Drug class
- Nasal Sprays
Timeline
| 21 Jul 2020 | Recall initiated by company | |
| 17 Aug 2020 | Classified by FDA | +27 days |
| 26 Aug 2020 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Superpotent Drug
Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.
Product as listed by the FDA
Desmopressin Acetate Nasal Spray 10 mcg/0.1 mL, 5mL glass vial with spray cap, Rx only, Manufactured for: AMRING PHARMACEUTICALS INC., Berwyn, PA 19312, NDC 69918-501-05
Where it was distributed
Nationwide within the United States.
Questions about this recall
Why was it recalled?
Superpotent Drug
Which lots are affected?
Lot #: N14695P, N14695S, exp. date 08 2020; N15627G , exp. date 10 2020 N15627GA, exp. date 10 2020 P10422A, exp. date 01 2021 P10422AA, exp. date 01 2021 P10430G, exp. date 03 2021 P11319M, exp. date 01 2021 P12969H, exp. date 05 2021 P12969IR, exp. date 05 2021 P13216G, exp. date 05 2021 P13216P, exp. date 05 2021 R11842A, exp. date 03 2022 R11842S, exp. date 03 2022 R12630A, exp. date 05 2022 R13071H, exp. date 04 2022
Where was it sold?
Nationwide within the United States.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 86066This product is part of a recall event; the main page for the event is Stimate (desmopressin acetate) Nasal Spray1.5 mg/mL glass recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Stimate (desmopressin acetate) Nasal Spray1.5 mg/mL glass recalled | Ferring Pharmaceuticals | Potency & Assay | Nationwide | |
| CLASS I | Ddavp Nasal Spray (desmopressin acetate) 10 mcg recalled | Ferring Pharmaceuticals | Potency & Assay | Nationwide |
More recalls from Ferring Pharmaceuticals
All 12| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Endometrin (progesterone) Vaginal Insert 100mg recalled | Ferring Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Zoma-Jet 5 Demonstration Kit recalled by Ferring Pharmaceuticals | Ferring Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Zoma-Jet 10 Demonstration Kit recalled by Ferring Pharmaceuticals | Ferring Pharmaceuticals | Other | Nationwide |
| Drug | CLASS III | Menopur 75 IU, (menotropins for injection) recalledMenopur | Ferring Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS I | Ddavp Nasal Spray (desmopressin acetate) 10 mcg recalled | Ferring Pharmaceuticals | Potency & Assay | Nationwide |
Other Desmopressin recalls
All 13| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Desmopressin Nasal Spray, USP, 10 mcg/ bottle (50 doses) recalled | Apotex | Other | Nationwide |
| Drug | CLASS II | Desmopressin Acetate Tablet, 0.2 mg recalled by RemedyRepack | RemedyRepack | Potency & Assay | MI |
| Drug | CLASS II | Desmopressin Acetate Tablets 0.2mg recalled by Heritage PharmaceuticalsDesmopressin Acetate | Heritage Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Desmopressin Acetate Tablets, 0.2 mg recalled | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | TX |
| Drug | CLASS II | Desmopressin Acetate Injection USP, 4 mcg/mL Preserved Vial recalled | Teva Pharmaceuticals USA | Sterility | Nationwide |