Progesterone 100 mg SR Capsules Recalled for Lack of Processing Controls
Duren Health Mart Pharmacy is recalling 1,306 capsules of Progesterone 100 mg SR due to a lack of processing controls.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Duren Health Mart Pharmacy is recalling 1,306 capsules of Progesterone 100 mg SR capsules (NDC 00311-2003-01). The recall was initiated because of a lack of processing controls.
The affected product was distributed only in Tennessee. The source text does not specify the exact dates of distribution or the number of patients affected.
Consumers who have this product should contact their healthcare provider or pharmacist for instructions on how to dispose of the medication or obtain a replacement.
The recalled product
- Product
- Progesterone 100 mg SR capsules, 30-180 capsules per prescription, Rx only, Duren's Health Mart Pharmacy 215 Dexter Woods Blvd. Waynesboro, TN38485, NDC 00311-2003-01
- Manufacturer
- Duren Health Mart Pharmacy
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 1,306
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- N/A
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 6 recalled by Duren Health Mart Pharmacy under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 6 products in this recall →Related recalls
Same manufacturer · Duren Health Mart Pharmacy
See all →- ModerateDuren Health Mart Pharmacy Recalls Omeprazole Suspension Due to Processing Controls
FDA (Drugs) · 2019-02-06
- ModerateTestosterone Cream Recalled for Lack of Processing Controls
FDA (Drugs) · 2019-02-06
- ModeratePromethazine Gel Recalled by Duren Health Mart Pharmacy for Processing Control Issues
FDA (Drugs) · 2019-02-06
- ModerateDomperidone 10 mg Capsules Recalled for Lack of Processing Controls
FDA (Drugs) · 2019-02-06
- ModerateProgesterone Cream Recalled for Lack of Processing Controls
FDA (Drugs) · 2019-02-06
Same hazard · processing controls
See all →- HighCompounded tirzepatide 8.8 mg vials recalled over lack of processing controls
FDA (Drugs) · 2025-08-13
- HighCompounded tirzepatide 11.24 mg vials recalled over lack of processing controls
FDA (Drugs) · 2025-08-13
- HighCompounded semaglutide 0.22 mg vials recalled over lack of processing controls
FDA (Drugs) · 2025-08-13
- HighCompounded semaglutide 0.44 mg vials recalled over lack of processing controls
FDA (Drugs) · 2025-08-13
- HighCompounded tirzepatide 4.4 mg vials recalled over lack of processing controls
FDA (Drugs) · 2025-08-13