State

Missouri product recalls

20,364 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri specifically in their distribution scope.

About recalls in Missouri

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Missouri consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15301–15325 of 20364

ModerateFDA (Drugs)·D-0012-2023·2022-10-26
Rifampin Capsules recalled due to excess nitrosamine impurity
Golden State Medical Supply Inc. is recalling Rifampin Capsules, 150 mg, due to elevated levels of 1-Methyl-4-Nitrosopiperazine (MNP) exceeding the FDA interim specification limit of 5 ppm. Affected lots are distributed nationwide.
Product
Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30
Category
Drug
Distribution
Distributed nationwide
HighCPSC·23022·2022-10-25
Pine-Sol Multi-Surface and All-Purpose Cleaners Recalled for Bacterial Contamination
Clorox is recalling Pine-Sol cleaners contaminated with Pseudomonas aeruginosa, a bacteria that risks serious infection in immunocompromised people or those with external medical devices. No illnesses have been reported to date.
Product
Pine-Sol® Scented Multi-Surface Cleaners in Lavender Clean®, Sparkling Wave®, and Lemon Fresh scents, CloroxPro® Pine-Sol® All Purpose Cleaners, in Lavender Clean®, Sparkling Wave®, Lemon Fresh, and Orange Energy® scents, and Clorox® Professional™ Pine-Sol® Lemon Fresh Cleaners.
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23020·2022-10-20
Birds Choice Acrylic Bird Baths Recalled for Fire Hazard
Backyard Nature Products is recalling Birds Choice acrylic bird baths because sunlight concentrated through the acrylic can overheat nearby wooden surfaces like siding or decking, creating a fire hazard. Two reports of overheating, smoking, fire, and scorching have been received; no injuries reported.
Product
Birds Choice Hanging and Pole-Mounted Acrylic Bird Baths
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23703·2022-10-20
Juvo Plus Children's Butterfly Net Sets and Army Playsets Recalled for Lead and Phthalate Contamination
Juvo Plus is recalling butterfly net sets and army action figure playsets because components contain lead and phthalates above federal limits. These chemicals are toxic if ingested by young children and can cause health problems.
Product
Butterfly Net Sets and Army Action Figure Playsets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23019·2022-10-20
Gel Blaster SURGE 1.0 toy guns recalled due to fire hazard
Gel Blaster is recalling about 62,700 SURGE Model 1.0 toy guns because the lithium-ion battery pack can overheat and ignite. Thirty reports of smoking or fire have been received with no injuries reported.
Product
Gel Blaster SURGE 1.0 toy guns
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23018·2022-10-20
Mittal International Baby Blankets Recalled for Choking and Strangulation Hazard
TJX is recalling about 108,000 Mittal International baby blankets sold nationwide from September 2021 through July 2022 because loose threads can detach and pose choking, entrapment, and strangulation hazards to infants.
Product
Mittal International Baby Blankets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23021·2022-10-20
AQUALUNG Apeks Exotec SCUBA Buoyancy Compensators Recalled for Drowning Hazard
AQUALUNG is recalling Apeks Exotec SCUBA diving buoyancy compensator devices because the dump valve knob can get stuck when inflated, preventing the device from fully inflating and creating a drowning hazard. Approximately 330 units sold nationwide from August 2021 through June 2022 are affected.
Product
Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0052-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit Recalled for Mislabeled Expiration Dates
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent kits with incorrect expiration dates on the label, which extends the stated shelf life and could allow use of expired devices.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0030-2023·2022-10-19
Hobbs Helical Retrieval Basket Recall Due to Incorrect Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets (Catalog 4822) with incorrect expiration dates on device labels. The mislabeled dates extend the shelf life, risking use of expired devices that may not perform as intended.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4822
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0044-2023·2022-10-19
Biliary Pigtail Stent Kits Recalled Due to Incorrect Expiration Date Labels
Hobbs Medical recalls Biliary Pigtail Stent Kits with labeling showing incorrect expiration dates that extend the shelf life. Affected kits were distributed to US and international customers from March 2018 to September 2020.
Product
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0015-2023·2022-10-19
Hobbs Medical Polypectomy Snare recalled for incorrect expiration date on label
Hobbs Medical is recalling its Polypectomy Snare for an incorrect expiration date on the label that extends shelf life. Affected devices were distributed in the US and other countries from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4563
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0039-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled for incorrect expiration date
Hobbs Medical recalls biliary stent kits with incorrect expiration dates that extend shelf life. The kits were distributed from 2018 to 2020 in the US and select countries.
Product
Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0078-2023·2022-10-19
Olympus VC-10 Vacuum Curettage System Recalled for Incompatible Accessories
Olympus recalls the VC-10 Vacuum Curettage System due to serious injury risk from incompatible collection canisters. The FDA warns users against using accessories not listed in the device's instructions.
Product
Berkeley VC-10 Vacuum Curettage System, Model No. VC-10. For transcervical aspiration of the uterine cavity.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0056-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Medical Device Recalled for Mislabeled Expiration Date
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates that extend shelf life, affecting devices distributed in the US and five other countries from 2018 to 2020.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6534
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0050-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kits Recalled Due to Incorrect Expiration Dates
Freeman Pancreatic Flexi-Stent Kits are recalled due to device labels displaying incorrect expiration dates that extend shelf life. Affected units were distributed in the US and select countries from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catalog Number: 6503
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0061-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates
Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6566
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0012-2023·2022-10-19
Hobbs Medical Flex-Ez Guide Wire With Incorrect Expiration Date
Hobbs Medical Flex-Ez Guide Wire devices were labeled with an incorrect expiration date that extends shelf life beyond the intended duration. Affected devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0024-2023·2022-10-19
Hobbs Posi-Stop Injection Needles Recalled for Incorrect Expiration Date Labeling
Hobbs Medical, Inc. is recalling Posi-Stop Injection Needles with lot numbers ending in 'R' due to incorrect expiration dates on device labels. The mislabeling extends the apparent shelf life, potentially allowing use of expired sterile devices.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0058-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Distributed with Incorrect Expiration Date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on the device labels. Affected units distributed in the US and internationally from March 2018 to September 2020 may have been used beyond their actual safe shelf life.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6544
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0082-2023·2022-10-19
Prismaflex M Set Medical Device Recalled Due to Instruction Mistranslation
Baxter Healthcare is recalling 334,932 Prismaflex M Set M150 devices due to a mistranslation in instructions that creates contradictory information about patient body weight restrictions.
Product
Prismaflex M Set: M150 (product code 109990). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0069-2023·2022-10-19
Hobbs Medical Polypectomy Snare with Incorrect Expiration Date Label
Hobbs Medical is recalling Polypectomy Snare model 4565-OLY due to incorrect expiration dates on device labels that extend the product's shelf life. Affected devices were distributed between March 2018 and September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4565-OLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0037-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration dates
Hobbs Medical is recalling certain Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual validity. Affected devices distributed between March 2018 and September 2020 may be used beyond their true expiration date.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0051-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit Recalled for Mislabeled Expiration Date
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kit units with incorrect expiration dates on labels, extending apparent shelf life. Units distributed in the US and Canada, Austria, Belgium, Finland, and Norway from 2018–2020 are affected.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0084-2023·2022-10-19
Prismaflex ST Renal Therapy Sets Recalled for Mistranslated Safety Instructions
Baxter Healthcare is recalling 1,068,560 Prismaflex ST renal replacement therapy sets nationwide. The recall is due to a mistranslation in the Estonian instructions that contains contradictory information about patient weight restrictions.
Product
Prismaflex ST Set: ST60 (product code 107643), ST100 (product code 107636), ST150 (product code 107640). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0062-2023·2022-10-19
Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date labeling
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The labeling error extends the stated shelf life, potentially allowing use of degraded devices.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6567
Category
Medical Device
Distribution
Distributed nationwide