State

Missouri product recalls

73,827 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,501
Critical: 1,339
Severe: 2,204
Most recent: 2026-11-04

Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53326–53350 of 82328

SevereFDA (Drugs)·D-1258-2016·2016-07-20
Pharmakon Recalls Fentanyl and Ropivacaine Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 150 bags of compounded Fentanyl Citrate and Ropivacaine HCI injection due to a lack of assurance of sterility.
Product
Fentanyl Citrate 2 mcg/mL/Ropivacaine HCI 0.2% injection in 0.9% Sodium Chloride, 100 mL bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0029-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1334-2016·2016-07-20
Pharmakon Recalls Ondansetron Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 2,300 units of compounded Ondansetron 2mg/mL syringes because the company cannot ensure the product is sterile.
Product
Ondansetron 2mg/mL, 2 mL fill in a 3 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0957-69
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1231-2016·2016-07-20
Medaus Recalls Niacinamide Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of Niacinamide 100 mg/mL vials because the company cannot guarantee the product's sterility.
Product
NIACINAMIDE 100 MG/ML (PF), In a) 1ML Vials, b) 5ML Vials, and c) 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1336-2016·2016-07-20
Pharmakon Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling Ephedrine Sulfate 5 mg/mL syringes because the company cannot guarantee the products are sterile.
Product
Ephedrine Sulfate 5 mg/mL in 0.9% Sodium Chloride, 10 mL BD syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0961-72
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1296-2016·2016-07-20
Pharmakon Recalls Oxytocin Infusion Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 1,809 units of compounded Oxytocin infusion bags nationwide due to a lack of assurance of sterility.
Product
Oxytocin 20 Units added to 0.9% Sodium Chloride in a 1000mL lntravia bag, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0740-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1194-2016·2016-07-20
Medaus Recalls L-Carnitine Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of L-Carnitine 100mg/mL vials because the company cannot ensure the product is sterile.
Product
L-CARNITINE 100MG/ML (PF), 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1291-2016·2016-07-20
Pharmakon Recalls Fentanyl Citrate Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling Fentanyl Citrate syringes because the company cannot ensure the products are sterile.
Product
Fentanyl Citrate 25mcg/mL in 0.9% Sodium Chloride 30 mL fill in a 35 mL Monoject Plungerless Syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0683-68
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2139-2016·2016-07-20
Hospira Recalls LifeCare PCA Plus II Infusion Pumps Due to Occlusion Detection Failure
Hospira is recalling 53,151 LifeCare PCA Plus II infusion pumps because wear on a component may prevent the detection of distal occlusions, resulting in serious injury.
Product
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through the intravenous or epidural routes in a wide range of clinical settings, including ICU, CCU, SICU, trauma units, bone marrow transplant centers, burn units…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1290-2016·2016-07-20
Pharmakon Recalls Provocholine Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 142 units of Provocholine pre-diluted syringes nationwide due to a lack of assurance of sterility.
Product
Provocholine pre-diluted in 0.9% Sodium Chloride Set II syringes, 0.0625mg/mL,3 mL; 0.25 mg/mL 3mL; 1 mg/mL 3mL; 4 mg/mL 3mL; 16 mg/ml 3mL, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0674-80
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1262-2016·2016-07-20
Pharmakon Recalls Hydromorphone Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 12 units of Hydromorphone HCl injection due to a lack of assurance of sterility. The product was distributed nationwide and to specific VA/DOD facilities.
Product
Hydromorphone HCl 1mg/ml injection in 0.9% Sodium Chloride, 100 mL Cadd Cassette (grey), Rx Only,Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0114-48
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1316-2016·2016-07-20
Pharmakon Recalls Morphine Sulfate Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 300 bags of Morphine Sulfate 1mg/mL due to a lack of assurance of sterility. The product was distributed nationwide and to specific VA/DOD facilities.
Product
Morphine Sulfate 1mg/mL (Preserved) in 0.9% Sodium Chloride, 50 mL lntravia bag, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0876-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1275-2016·2016-07-20
Pharmakon Recalls Promethazine IV Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 725 units of compounded Promethazine IV bags due to a lack of assurance of sterility. The products were distributed nationwide and to specific VA/DOD facilities.
Product
Promethazine 12.5mg added to 0.9% Sodium Chloride 50 mL fill in a 100 mL B/Braun PAB bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0186-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1635-2016·2016-07-20
Dr. Praeger's Recalls Quinoa Cowboy Veggie Burgers for Listeria Risk
Dr. Praeger's is voluntarily recalling Trader Joe's Quinoa Cowboy Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Product
Trader Joe's Quinoa Cowboy Veggie Burger, 26 x 12 oz. (340g)/box, Best if used by: May-12-2018, UPC 0053 2761, Dist. & Sold Exclusively By: Trader Joe's, Monrovia CA 91016
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1181-2016·2016-07-20
Medaus Recalls DMSO 99.9 Vials Due to Sterility Concerns
Medaus, Inc. is recalling DMSO 99.9 vials because the company cannot ensure the product is sterile. The recall covers 5 mL and 10 mL vials distributed in the U.S., Japan, and New Zealand.
Product
DMSO 99.9 (PF), In a) 5ML Vials and b) 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1299-2016·2016-07-20
Pharmakon Recalls Oxytocin Lactated Ringers Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 384 units of compounded Oxytocin in Lactated Ringers due to a lack of assurance of sterility.
Product
Oxytocin 20 Units added to Lactated Ringers in a 1000 mL lntravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0769-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1333-2016·2016-07-20
Pharmakon Recalls Rocuronium Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 1,925 vials of Rocuronium 10 mg/mL syringes because the company cannot guarantee the product is sterile.
Product
Rocuronium 10 mg/mL, 5 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0955-70
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1359-2016·2016-07-20
Hospira Recalls Diazepam Injection Due to Crystallized Active Ingredient
Hospira Inc. is recalling 373,850 tubes of Diazepam Injection USP 10mg/2mL because the product contains particulate identified as crystallized active ingredient.
Product
DIAZEPAM — DIAZEPAM (DIAZEPAM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1630-2016·2016-07-20
Dr. Praeger's Recalls Frozen Veggie Burgers Due to Listeria Risk
Dr. Praeger's is voluntarily recalling Jumbo California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Product
Dr. Praeger's Purely Sensible Foods Jumbo California Veggie Burger (Vegan), 5.5 oz., 10 lbs (4.54.kg), Best if used by: May 17, 2018, UPC (01) 00080868 01011, Dr. Praegers Sensible Foods, Elmwood Park, NJ 07407
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1242-2016·2016-07-20
Medaus Recalls Testosterone Cypionate Vials Due to Sterility Concerns
Medaus, Inc. is recalling Testosterone Cypionate vials because the company cannot guarantee the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Product
TESTOSTERONE CYP 200 MG/ML W/PRES (BENZYL ETOH 2%), In a) 1ML Vials, b) 2ML Vials, c) 3ML Vials, d) 4ML, and e) 5ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1304-2016·2016-07-20
Pharmakon Recalls Hydromorphone PCA Vials Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 670 vials of compounded Hydromorphone HCl 0.4mg/ml due to a lack of assurance of sterility. The products were distributed nationwide to VA and DOD facilities.
Product
HYDROmorphone HCI 0.4mg/ml in 0.9% Sodium Chloride, 30 mL PCA Vial, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0813-68
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1642-2016·2016-07-20
Dr. Praeger's Recalls Frozen Veggie Burgers Due to Listeria Risk
Dr. Praeger's Sensible Foods is voluntarily recalling specific frozen veggie burgers because they may be contaminated with Listeria monocytogenes.
Product
Dr. Praeger's Bombay Veggie Burgers, 6 x 10 oz. (283g)/box, Best if used by: May-12-2018, UPC (01) 6 0080868 000050 5, Dr. Praeger's Sensible Foods, Elmwood Park, NJ 07407
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1179-2016·2016-07-20
Medaus Recalls Dexpantenol Vials Due to Lack of Sterility Assurance
Medaus, Inc. is recalling Dexpantenol 250mg/mL vials because the company cannot ensure the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Product
DEXPANTHENOL 250MG/ML W/PRES. (BENZALKONIUM CHL 0.01%), 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1188-2016·2016-07-20
Medaus Recalls Hyaluronidase Vials Due to Sterility Assurance Concerns
Medaus, Inc. is recalling Hyaluronidase 500U/ML vials because the company cannot assure the sterility of the product. The recall affects lots distributed in the U.S., Japan, and New Zealand.
Product
HYALURONIDASE 500U/ML(PF), 3ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1276-2016·2016-07-20
Pharmakon Recalls Promethazine Compounded Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 485 units of compounded Promethazine 25 mg in 0.9% Sodium Chloride bags due to a lack of assurance of sterility.
Product
Promethazine 25 mg added to 0.9% Sodium Chloride 50 mL fill in a 100 mL B/Braun PAB bag, Rx, Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0187-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1230-2016·2016-07-20
Medaus Recalls Nandrolone Decanoate Vials Due to Sterility Concerns
Medaus, Inc. is recalling Nandrolone Decanoate 200mg/mL vials because the company cannot guarantee the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Product
NANDROLONE DEC 200MG/ML W/PRES. (BENZYL ETOH 10%), In a) 2ML Vials, b) 4ML Vials, and c) 5ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide