State

Missouri product recalls

73,218 recalls have nationwide distribution and so reach Missouri. 8,493 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,493
Critical: 1,344
Severe: 1,882
Most recent: 2026-09-23

Of the 8,493 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,882 (22%) are Severe.

Which agencies issued them

These figures cover only the 8,493 recalls whose distribution notice names Missouri specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15951–15975 of 81711

HighFDA (Devices)·Z-2254-2023·2023-08-09
Zimmer Periarticular Locking Plate recalled due to thread form defect
Zimmer Periarticular Locking Plates have a thread form defect that prevents surgical screws from properly mating with the plate. 75 units distributed across multiple U.S. states and internationally.
Product
Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary internal fixation and stabilization of osteotomies and fractures, including comminuted fractures, supracondylar fractures, intra-articular and extra-articular…
Category
Medical Device
Distribution
10 states
HighFDA (Drugs)·D-1043-2023·2023-08-09
Fentanyl injection syringes recalled for unvalidated sterilization process
Central Admixture Pharmacy Services is recalling 5,124 fentanyl syringes because the manufacturer lacks validation that its sterilization process is effective. The nationwide recall affects multiple lot numbers distributed through September 2023.
Product
fentaNYL, 1250 mcg/25 mL, (50 mcg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-7
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1044-2023·2023-08-09
HYDROmorphone Injectable Syringes Recalled Due to Sterility Assurance Concerns
Central Admixture Pharmacy Services Inc is recalling HYDROmorphone injectable syringes because sterilization cycles were not validated. The recall affects 2,717 units distributed nationwide.
Product
HYDROmorphone in 0.9% sodium chloride, 6 mg/30 mL, (0.2 mg/mL), 30 mL Syringe, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2010-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2326-2023·2023-08-09
FDA Recalls Medline Procedural Kits Due to Potential Sterility Failure
Medline Industries is recalling 22 procedural kits because the included ultrasound gel may not be sterile as labeled. The kits were distributed worldwide.
Product
Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PREMIUM CLOSUREPLUS PACK, Model Number: DYNJ54326A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2317-2023·2023-08-09
Medline Procedural Kits Recalled for Ultrasound Gel Sterility Defect
Medline Industries recalled 11,436 procedural kits with Turkuaz ultrasound gel that may not meet sterility specifications. The affected kits were distributed worldwide from April 2020 to April 2023.
Product
Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. (54) KIT STC PLASTIC FREE FLAP, Model Number: DYNJ909031; b. BREAST, Model Number: DYNJ904598B; c. BREAST DBL PROCED SUPPLEMENT, Model Number: DYNJ63893…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1074-2023·2023-08-09
Lidocaine Injectable Syringes Recalled for Sterilization Assurance Concerns
CAPS Inc. is recalling 9,517 lidocaine 2% injectable syringes distributed nationwide due to lack of sterilization validation data. No illnesses have been reported.
Product
lidocaine 2%, 100 mg /5 mL, (20 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6006-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0962-2023·2023-08-09
FDA Recalls Phenylephrine IV Bags Due to Lack of Sterility Assurance
Central Admixture Pharmacy Services is recalling phenylephrine IV bags nationwide due to insufficient sterility assurance and lack of validation data for decontamination cycles used in manufacturing.
Product
phenylephrine, 25mg added to 0.9% sodium chloride 250 mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-7011-1.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1060-2023·2023-08-09
HYDROmorphone Injectable Syringes Recalled for Lack of Sterilization Validation
Central Admixture Pharmacy Services is recalling 5,259 HYDROmorphone injectable syringes nationwide due to lack of validation data for sterilization, raising concerns about product sterility assurance.
Product
HYDROmorphone in 0.9% sodium chloride, 30 mg/30 mL, (1 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2012-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2269-2023·2023-08-09
SPiN Xtend Instruments Recalled for Electromagnetic Sensor Tracking Malfunction
Olympus Corporation is recalling 144 units of SPiN Xtend 2.0mm OD instruments (Model INS-5450) due to electromagnetic sensor tracking malfunction that impairs navigation during endobronchial procedures and may cause procedural delays.
Product
Always-On Tip Tracked Instruments (SPiN Drive instruments) SPiN Xtend 2.0mm OD, 21ga Intended for use in clinical interventions and for anatomical structures where computed tomography and/or endoscopic brINS-0362onchoscopy are currently used for visualizing Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1047-2023·2023-08-09
Fentanyl Injectable Syringes Recalled Due to Sterility Assurance Failure
Central Admixture Pharmacy Services is recalling 1,216 fentanyl 2500 mcg/50 mL syringes distributed nationwide due to lack of validation data for sanitization cycles, which cannot assure sterility.
Product
fentaNYL, 2500 mcg/50 mL, (50 mcg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-3
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1063-2023·2023-08-09
Fentanyl Injectable Recalled for Lack of Sterility Assurance
Central Admixture Pharmacy Services is recalling 1,044 bags of fentanyl injectable solution due to lack of validated sanitization procedures that could compromise sterility assurance. The product affects healthcare facilities nationwide.
Product
fentaNYL in 0.9% sodium chloride, 5000 mcg/250 mL, (20 mcg/mL), 250 mL Bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2074-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0990-2023·2023-08-09
Potassium Phosphate IV Bags Recalled for Lack of Sterility Assurance
Central Admixture Pharmacy Services is recalling potassium phosphate intravenous bags due to lack of sterility assurance and missing validation data for decontamination processes. The recall affects 234 bags distributed nationwide.
Product
potassium phosphate, 30 mmole added to 0.9% sodium Chloride 500mL, IV Bag, RX Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-7016-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0946-2023·2023-08-09
Prescription oral drug solution recalled due to manufacturing quality deviation
The Ritedose Corporation is recalling Cromolyn Sodium Oral Solution (Concentrate) due to a manufacturing deviation. Lot 23CE2, distributed nationwide, was released prior to obtaining required supplier approval.
Product
Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2249-2023·2023-08-09
Gore Tips Set Device Recall: Incorrect Expiration Date Labeling
Creganna Medical Devices is recalling three lots of Gore Tips Set Device due to incorrect expiration date labeling. Affected devices may be used past their actual expiration date.
Product
Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2251-2023·2023-08-09
Surgical table drapes and infection control kits recalled for naphthalene odor
Microtek Medical Inc. is recalling certain lots of surgical table drapes and infection control kits due to detection of naphthalene odor. The affected products are distributed nationwide in the US and in Canada.
Product
Equipment and table drapes and Surgical Room Turnover (SRT) Kits: (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile; (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2250-2023·2023-08-09
Ecolab Medical Device Drapes Recalled for Naphthalene Odor
Microtek Medical Inc. is recalling certain lots of Ecolab sterile medical device drapes due to naphthalene odor. The recall affects five models distributed in the United States and Canada.
Product
Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape, 91 cm x 51 cm (36 in x 20 in), Model 63620RT, pkgd. 25/case, sterile; (2) Ecolab Microtek Banded Bag with Elastic Opening, Circular, 102 cm (40 in), Model 60040S, pkgs. 25/case, sterile; (3) Ecolab…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V561000·2023-08-08
Explorer Van Company Recalls 2020-2022 GMC Savana and Ford Transit Vans
Explorer Van Company is recalling certain 2020-2022 upfitted GMC Savana and 2020 Ford Transit vans because an improperly secured fuel hose may cause a gas leak and increase fire risk.
Product
EXPLORER VAN COMPANY — EXPLORER VAN COMPANY GMC SAVANNA, FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V560000·2023-08-08
Hino Recalls 2020-2024 Conventional Models for Fuel Gauge Defect
Hino is recalling 8,025 vehicles because a fuel sensor defect may cause inaccurate readings, leading to unexpected stalling and increased crash risk.
Product
HINO — HINO CONVENTIONAL MODELS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V558000·2023-08-07
Forest River Recalls 2023 Pause Travel Trailers Due to Awning Defect
Forest River is recalling 2023 Pause travel trailers because the awning may not be adequately secured, posing a risk of injury or crash if it detaches.
Product
FOREST RIVER — FOREST RIVER PAUSE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V559000·2023-08-07
2024 Forest River Sierra and Sandpiper Braking System Defect
Forest River is recalling certain 2024 Sierra and Sandpiper fifth wheels due to backwards axle installation that reduces braking ability and increases crash risk. Dealers will reinstall the axle at no cost.
Product
FOREST RIVER — FOREST RIVER SANDPIPER, SIERRA
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-080723-01·2023-08-07
USDA Alerts on Fresh Salads and Wraps with Possible Lettuce Contamination
USDA FSIS issued a public health alert for Fresh Seasons Kitchen salads and wraps due to possible deer feces contamination in lettuce.
Product
FSIS Issues Public Health Alert for Fresh Salads and Wraps with Meat and Poultry due to Possible Lettuce Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·23V554000·2023-08-04
Mercedes-Maybach S 580 and S 680 Recalled for Trunk Wiring Defect
Mercedes-Benz is recalling 2022-2023 Maybach S 580 and S 680 vehicles because a loose 12-volt ground connection in the trunk may impair stability control or cause overheating.
Product
MERCEDES-MAYBACH — MERCEDES-MAYBACH S 580 4MATIC, S 680 4MATIC, S 680
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V555000·2023-08-04
Mercedes-Benz Recalls 2023 EQE Models for Roof Frame Absorber Defect
Mercedes-Benz is recalling 2023 EQE 350, EQE 500, and AMG EQE vehicles because roof frame absorbers may detach during airbag deployment, increasing injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ EQE 500, AMG EQE, redundant EQE 350 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-08042023-01·2023-08-04
USDA Issues Public Health Alert for Raw Beef Due to Plastic Contamination
USDA FSIS issued a public health alert for raw beef products that may contain soft, clear plastic. Consumers are urged not to consume the product.
Product
Cargill Meat Solutions Corporation — FSIS Issues Public Health Alert for Raw Beef Product Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·23V556000·2023-08-04
2024 Hyundai Tucson Recalled for Incorrect Tire Information Label
The tire and loading information label on 2024 Hyundai Tucson vehicles may provide incorrect spare tire information, potentially causing confusion during emergency tire replacement.
Product
HYUNDAI — HYUNDAI TUCSON
Category
Vehicle
Distribution
Distributed nationwide