MD-Gastroview — Class II drug recall D-1132-2015
Terminated recall by Mallinckrodt, Inc., reported 2015-06-17. Labeling: incorrect or missing lot number and/or expiration date
| Recall number | D-1132-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mallinckrodt, Inc., Hazelwood, MO, United States |
| Recall initiated | 2015-05-15 |
| Classified | 2015-06-10 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2017-07-10 |
| Countries outside the US | CR |
| Quantity | 6,600 bottles |
| Reason classes | labeling |
| NDC | 00019-4816, 00019-4816-04 |
| Lot numbers | B201B, B346D |
| Expiration dates | 2015-04-20, 2015-08-20 |
Product
MD-Gastroview (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP); 37% Organically Bound Iodine For Gastrointestinal Radiography; Oral or rectal use only; Rx only; 30 mL; Single-Unit Container; ; Mallinckrodt Inc., St. Louis, MO 63042. NDC 0019-4816-04
Reason for recall
Labeling: incorrect or missing lot number and/or expiration date
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1132-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.