FDA Drug recall D-0298-2019
SODIUM CHLORIDE INJECTION, USP, 0.9%, 10 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL…
- FDA Drug
- Class I
- terminated
- Published 2018-12-12
On 2018-12-12 the FDA classified a Class I recall of SODIUM CHLORIDE INJECTION, USP, 0.9%, 10 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL… by Fresenius Kabi Usa, citing labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due to an incorrect statement on the product insert for product codes 918610 and 918620 indicating that the….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0298-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-11-15 |
| Published | 2018-12-12 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Fresenius Kabi Usa |
| Distribution | US |
Product
SODIUM CHLORIDE INJECTION, USP, 0.9%, 10 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173. NDC 63323-186-10 Product code 918610
Reason
Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due to an incorrect statement on the product insert for product codes 918610 and 918620 indicating that the stoppers do not contain natural rubber latex. The tray label for these two product codes and the vial label for product code 918620 also incorrectly state that the stoppers do not contain latex. The above listed product codes and batches being recalled have stoppers containing natural rubber latex.
Identifiers
| ndc | 63323-186-04 |
|---|---|
| ndc | 63323-186-02 |
| ndc | 63323-186-01 |
| ndc | 63323-186-10 |
| ndc | 63323-186-03 |
| ndc | 63323-186-20 |
| code_info | Lot# EXP date: 6013112 11/2018 6013113 11/2018 6013114 11/2018 6013180 11/2018 6013181 11/2018 6013182 11…Lot# EXP date: 6013112 11/2018 6013113 11/2018 6013114 11/2018 6013180 11/2018 6013181 11/2018 6013182 11/2018 6013237 01/2019 6013238 01/2019 6013239 01/2019 6013468 02/2019 6013512 02/2019 6013513 02/2019 6013551 02/2019 6013552 02/2019 6013553 02/2019 6013607 02/2019 6013608 02/2019 6013610 02/2019 6013627 03/2019 6013678 03/2019 6013679 03/2019 6013822 03/2019 6013823 03/2019 6013824 03/2019 6013924 04/2019 6013925 04/2019 6013926 04/2019 6014003 05/2019 6014004 05/2019 6014005 05/2019 6014260 05/2019 6014301 05/2019 6014302 05/2019 6014303 06/2019 6014304 06/2019 6014305 06/2019 6014306 06/2019 6014307 06/2019 6014384 06/2019 6014404 06/2019 6014405 06/2019 6014453 06/2019 6014454 06/2019 6014455 06/2019 6014479 06/2019 6014557 07/2019 6014558 07/2019 6014606 07/2019 6014649 08/2019 6014650 08/2019 6014704 08/2019 6014766 08/2019 6014767 08/2019 6014768 08/2019 6014841 08/2019 6014842 08/2019 6014843 08/2019 6014861 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0298-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.