FDA Drug recall D-240-2013
TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Prescription Only
- FDA Drug
- Class III
- terminated
- Published 2013-04-10
On 2013-04-10 the FDA classified a Class III recall of TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Prescription Only by Ferring Pharmaceuticals, citing labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons labelled for Needle-Free Head B, but contaiin Needle-Free Head A.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-240-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-02-01 |
| Published | 2013-04-10 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Ferring Pharmaceuticals |
| Distribution | US |
Product
TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Prescription Only. Distributed By: TEVA Biologics & Specialty Products Division of Teva Pharmaceuticals USA, Sellersville, PA 18960 Manufactured in Israel.
Reason
Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons labelled for Needle-Free Head B, but contaiin Needle-Free Head A
Identifiers
| code_info | LOT #201131320087 Exp 09/15 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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All Ferring Pharmaceuticals recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-240-2013%22
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