State

Missouri product recalls

73,388 recalls have nationwide distribution and so reach Missouri. 8,494 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,494
Critical: 1,344
Severe: 2,198
Most recent: 2026-10-07

Of the 8,494 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 2,198 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,494 recalls whose distribution notice names Missouri specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20726–20750 of 81882

HighFDA (Devices)·Z-1681-2022·2022-09-14
ChemoLock Infusion Ports Recalled for Unintended Disconnection Risk
ICU Medical recalls ChemoLock chemotherapy infusion ports for potential unintended disconnection due to spring variation, which may delay therapy and expose patients to caustic substances.
Product
Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY SPIKE/CL-12; APPX 1.5ml,ChemoLock BAG SPIKE WITH ADDITIVE PORT/CL-13; ChemoLock Port/CL2100; ChemoLock Port, 5 Units/CL2100-5; ChemoLock Port/CL2100T; Clave Bag…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1692-2022·2022-09-14
PICC and Central Line Packs Exposed to Unvalidated Sterilization Cycles
American Contract Systems is recalling PICC line and central line packs due to exposure to multiple sterilization cycles without validation. Two units were distributed to healthcare facilities in 13 U.S. states.
Product
Various PICC Line, Central Line Packs
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1693-2022·2022-09-14
ENT Surgical Packs Recalled Due to Sterilization Validation Failure
American Contract Systems recalls various ENT surgical packs that may not have been properly sterilized due to multiple sterilization cycles without adequate validation. The packs were distributed to healthcare facilities in 13 states.
Product
Various ENT Packs
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1700-2022·2022-09-14
Neurology Surgical Packs Recalled for Sterilization Validation Failure
American Contract Systems recalls 37 units of neurology surgical packs distributed across 13 US states due to exposure to multiple sterilization cycles without proper validation.
Product
Various neurology packs
Category
Medical Device
Distribution
13 states
HighFDA (Food)·F-1686-2022·2022-09-14
King's Hawaiian Pretzel Buns Recalled for Potential Bacterial Contamination
King's Hawaiian pretzel hamburger buns, slider buns, and pretzel bites are recalled nationwide. An ingredient used in manufacturing may contain Cronobacter sakazakii or Clostridium botulinum.
Product
King's Hawaiian 10.5 oz. Pretzel Hamburger Buns (UPC 73435000365), 10.2 oz. Pretzel Bites (UPC 73435000525.), and 11 oz. Slider Buns (UPC 73435000372 ) packed in plastic bags. Distributed by King s Hawaiian Bakery West, Inc., 19161 Harborgate Way, Torrance, CA 90501
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1689-2022·2022-09-14
Angiography Packs Recalled Due to Sterilization Validation Failure
American Contract Systems, Inc. is recalling 57 angiography packs and trays that were exposed to multiple sterilization cycles without proper validation for repeated sterilization exposure.
Product
Various Angiography packs/trays
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1705-2022·2022-09-14
Eye Surgery Packs Recalled Due to Improper Sterilization Validation
American Contract Systems is recalling various eye and cataract surgery packs distributed to US health systems because the products were exposed to multiple sterilization cycles without validation. Unvalidated sterilization may compromise device sterility.
Product
Various eye packs, cataract packs
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1704-2022·2022-09-14
D&C Pack Recall Due to Sterilization Validation Failure
American Contract Systems is recalling D&C packs that were exposed to multiple sterilization cycles without proper validation. The sterilization failure may compromise device sterility.
Product
D&C pack
Category
Medical Device
Distribution
13 states
HighFDA (Drugs)·D-1491-2022·2022-09-14
Guaifenesin and Dextromethorphan Cough Syrup Recalled for Manufacturing Control Deviations
Plastikon Healthcare LLC is recalling Guaifenesin and Dextromethorphan cough syrup cups distributed nationwide due to manufacturing processes that were not adequately controlled.
Product
GUAIFENESIN AND DEXTROMETHORPHAN 200-20 mg/10 mL, 10 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6980-72
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V686000·2022-09-14
2022 Ford F-150 Parking Light Flickering Defect Recall
Ford is recalling 2022 F-150 trucks and 2022-2023 Bronco Sport vehicles due to a lighting control module defect causing parking light flickering when headlights are activated. The flickering reduces visibility and increases crash risk.
Product
FORD — FORD F-150, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1493-2022·2022-09-14
CORRECTDOSE Children's Pain Relief and Fever Reducer Acetaminophen Recalled for Manufacturing Control Violations
CORRECTDOSE Children's Fever Reducer (160 mg/5 mL acetaminophen) has been recalled due to manufacturing control deviations. The recall affects 1,464 units distributed nationwide.
Product
CORRECTDOSE Children's PAIN RELIEF & Fever Reducer, Cherry, (Acetaminophen 160 mg per 5 mL), 2.04 FL.OZ (60mL), packaged in 12-5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-311-05 UPC 8 60003 67145 0
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1703-2022·2022-09-14
C-Section Surgical Packs recalled for improper sterilization validation
American Contract Systems recalls C-section surgical packs that were exposed to multiple sterilization cycles without validation. The sterilization integrity of the 24 affected units cannot be assured.
Product
Various C-section packs
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1696-2022·2022-09-14
Port Insertion Packs Recalled Due to Unvalidated Sterilization
American Contract Systems is recalling Various Port Insertion Packs that were exposed to multiple sterilization cycles without proper validation. The devices may not meet sterility standards.
Product
Various Port Insertion Packs
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1697-2022·2022-09-14
Breast Abdominoplasty Pack Recalled for Inadequate Sterilization Cycle Validation
American Contract Systems, Inc. is recalling Breast Abdominoplasty Packs that were exposed to multiple sterilization cycles without validation that the process could safely maintain instrument sterility through repeated exposures.
Product
Breast Abdominoplasty Pack
Category
Medical Device
Distribution
13 states
HighFDA (Drugs)·D-1498-2022·2022-09-14
Difluprednate Eye Drops Recalled for Defective Container Compromising Sterility
CIPLA is recalling 3,468 bottles of Difluprednate Ophthalmic Emulsion nationwide due to defective protective caps that could expose the dropper tip and compromise sterility. No injuries have been reported.
Product
Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle, RX only, Manufactured for Exelan Pharmecuticals, Inc., Boca Raton, FL 33432, NDC 76282-708-50.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1495-2022·2022-09-14
Lidocaine Hydrochloride Jelly Recalled Due to cGMP Deviations and Turbidity
Akorn, Inc. is recalling 82,689 tubes of Lidocaine Hydrochloride Jelly USP, 2%, due to cGMP deviations and turbidity discovered during sterility testing. The recall affects multiple lots distributed nationwide.
Product
Lidocaine Hydrochloride Jelly USP, 2%, Sterile, 30mL tube, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-711-31
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2022·2022-09-14
External Fixation Wire May Fracture During Surgery, Leaving Fragments in Patient
OrthoPediatrics Corp is recalling an external fixation wire due to manufacturing variance that may cause the tip to fracture. Fractured fragments could remain in patients.
Product
Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1486-2022·2022-09-14
Acetaminophen Oral Solution Recalled for Manufacturing Process Control Failures
Plastikon Healthcare LLC is recalling acetaminophen oral solution (650 mg per 20.3 mL cup) distributed nationwide due to manufacturing process control failures.
Product
Acetaminophen Oral Solution 650 mg / 20.3 mL, 20.3 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6820-76
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V687000·2022-09-14
2022 Volkswagen Taos Engine Stall Software Safety Recall
Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.
Product
VOLKSWAGEN — VOLKSWAGEN TAOS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1677-2022·2022-09-14
CARTO VIZIGO Guiding Sheath Recalled Due to Water-Damaged Sterile Packaging
Biosense Webster is recalling 98 units of CARTO VIZIGO 8.5F guiding sheaths due to water damage to packaging that may have compromised the sterile barrier, creating a potential infection risk.
Product
CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1490-2022·2022-09-14
Guaifenesin and dextromethorphan liquid medication recalled for manufacturing control issues
Plastikon Healthcare LLC is recalling guaifenesin and dextromethorphan liquid medication (280,500 cups) distributed nationwide due to manufacturing control deviations in production.
Product
GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152. NDC 0904-6844-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2022·2022-09-14
Obstetric and gynecology surgical packs recalled for unvalidated sterilization exposure
American Contract Systems is recalling 15 obstetric and gynecology surgical packs that underwent multiple sterilization cycles without validation. This could compromise product sterility and increase infection risk during procedures.
Product
Various ob/gyn packs
Category
Medical Device
Distribution
13 states
HighFDA (Drugs)·D-1492-2022·2022-09-14
CORRECTDOSE Children's Allergy Relief Recalled Due to Manufacturing Process Control Deviations
CORRECTDOSE Children's Allergy Relief (Diphenhydramine HCl 12.5 mg per 5 mL) is being recalled nationwide. The FDA determined products were manufactured under conditions with inadequate process control.
Product
CORRECTDOSE Children's ALLERGY RELIEF (Diphenhydramine HCl 12.5 mg per 5 mL), 2.04 FL. OZ (60 mL) packaged in 12- 5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-302-05 UPC 8 60003 67144 3
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1484-2022·2022-09-14
Acetaminophen Oral Solution 160 mg Recalled for Manufacturing Control Deviations
Acetaminophen Oral Solution 160 mg/5 mL (290,270 cups) recalled nationwide due to CGMP manufacturing control deviations. Product was distributed to institutional healthcare facilities.
Product
Acetaminophen Oral Solution 160 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6738-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2022·2022-09-14
Early Bird Bleed Monitoring System Introducer fails to power on
Saranas, Inc. is recalling 953 units of the Early Bird Bleed Monitoring System Introducer Sheath Set due to a design error that prevents the device from powering on and completing self-tests. The product was distributed nationwide.
Product
Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
Category
Medical Device
Distribution
Distributed nationwide