Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31
cGMP deviations.
- Agency
- FDA Drug
- Recall date
- Apr 1, 2026
- Status
- Ongoing
- Company
- Wells Pharma of Houston LLC
1. What product was recalled?
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
Quantity: 4975 syringes
Code or lot text: 120925302312764, Exp Date 04/09/2026, 123125302312879 Exp Date, 05/05/2026, 123125302312880, Exp Date 05/05/2026, 010226302310003, Exp Date 05/06/2026, 010626302310007, Exp Date 05/08/2026, 010626302310008, Exp Date 05/08/2026 020426302310243, Exp Date 06/06/2026.
- LOT
- 010226302310003
- LOT
- 010626302310007
- LOT
- 010626302310008
- LOT
- 05/05/2026
- LOT
- 120925302312764
- LOT
- 123125302312879 Exp Date
- LOT
- 123125302312880
- LOT
- Exp Date 04/09/2026
- LOT
- Exp Date 05/05/2026
- LOT
- Exp Date 05/06/2026
- LOT
- Exp Date 05/08/2026
- LOT
- Exp Date 05/08/2026 020426302310243
- LOT
- Exp Date 06/06/2026.
- RECALL-NUMBER
- D-0507-2026
fentaNYL Citrate Injectable Solution in 0
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.
Quantity: 150 syringes
Code or lot text: Lot 022326203650432; Exp Date 06/25/2026
- LOT
- Exp Date 06/25/2026
- LOT
- Lot 022326203650432
- RECALL-NUMBER
- D-0506-2026
fentaNYL Citrate injectable Solution in 0
fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg per mL), 250 mL bag, wells pharma of Houston, NDC 73702-202-03.
Quantity: 2940 IV Bags
Code or lot text: 120125202032701, Exp Date 04/01/2026; 122625202032857, Exp Date 04/25/2026; 122625202032862, Exp Date 04/28/2026, 122625202032863. Exp Date 04/28/2026; 122625202032864, Exp Date 04/28/2026; 122625202032865, Exp Date 04/28/2026, 011226202030062, Exp Date 05/14/2026, 011326202030776, Exp Date 05/15/2026; 011326202030077, Exp Date 05/15/2026, 011626202030111, Exp Date 05/20/2026, 011926202030122, Exp Date 05/21/2026; 011926202030123, Exp Date 05/21/2026, 012726202030159, Exp Date 05/28/2026, 020226202030200, Exp Date 06/04/2026, 020326202030216, Exp Date 06/05/2026, 020426202030234, Exp Date 06/06/2026, 02182202030398, Exp Date 06/20/2026.
- LOT
- 011226202030062
- LOT
- 011326202030077
- LOT
- 011326202030776
- LOT
- 011626202030111
- LOT
- 011926202030122
- LOT
- 011926202030123
- LOT
- 012726202030159
- LOT
- 020226202030200
- LOT
- 020326202030216
- LOT
- 020426202030234
- LOT
- 02182202030398
- LOT
- 120125202032701
- LOT
- 122625202032857
- LOT
- 122625202032862
- LOT
- 122625202032863. Exp Date 04/28/2026
- LOT
- 122625202032864
- LOT
- 122625202032865
- LOT
- Exp Date 04/01/2026
- LOT
- Exp Date 04/25/2026
- LOT
- Exp Date 04/28/2026
- LOT
- Exp Date 05/14/2026
- LOT
- Exp Date 05/15/2026
- LOT
- Exp Date 05/20/2026
- LOT
- Exp Date 05/21/2026
- LOT
- Exp Date 05/28/2026
- LOT
- Exp Date 06/04/2026
- LOT
- Exp Date 06/05/2026
- LOT
- Exp Date 06/06/2026
- LOT
- Exp Date 06/20/2026.
- RECALL-NUMBER
- D-0504-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
cGMP deviations.
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Drug source
Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.