State

Missouri product recalls

20,305 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.

11926–11950 of 20305

SevereFDA (Devices)·Z-2386-2023·2023-08-23
MAHURKAR dialysis catheters recalled for center lumen occlusion risk
Covidien LP recalls MAHURKAR dialysis catheters due to excessive silicone lubricant on the catheter tip, which can obstruct the center lumen. This may delay treatment and cause serious blood complications including embolism and thrombosis.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, Kit" REF: 8888345611
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2378-2023·2023-08-23
Dialysis catheter recall: excessive lubricant causes center lumen obstruction
A dialysis catheter product is being recalled due to excessive lubricant coating in the center lumen, which may cause full or partial obstruction. The blockage could delay treatment and increase risk of blood clots and hemolysis.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2371-2023·2023-08-23
Dialysis Catheters Recalled for Catheter Obstruction from Excessive Silicone Lubricant
Covidien is recalling 1,875 MAHURKAR dialysis catheters with lot numbers 2204000239 and 2227800110 due to excessive silicone lubricant causing catheter obstruction. The obstruction may delay treatment or cause hemolysis and thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, IC Tray REF: 8888102003HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2377-2023·2023-08-23
Acute Dialysis Catheters Recalled for Catheter Tip Occlusion
Covidien recalls 519 MAHURKAR acute dialysis catheters (Lot 2200400292) due to excessive silicone lubricant coating the catheter tip that may cause partial or full occlusion and treatment delays.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, PASS Tray REF: 8888104004HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2374-2023·2023-08-23
Dialysis Catheter Recall: Center Lumen Occlusion Due to Excessive Lubricant
Covidien LP is recalling MAHURKAR 12 Fr dialysis catheters due to center lumen occlusion from excessive lubricant. The defect may cause treatment delays and serious complications including embolism and thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, PASS Tray REF: 8888103002HP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2023·2023-08-23
Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm
Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.
Product
CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2414-2023·2023-08-23
FreeStyle Libre 2 Readers may fail to activate new sensors
FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.
Product
FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2401-2023·2023-08-23
UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage
Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.
Product
UroPass Ureteral Access Sheaths, 5 pieces/box
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2407-2023·2023-08-23
Centurion FMS Pak Recalled Due to Patient Injury Risk from Plastic Debris
Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.
Product
Centurion FMS Pak
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2413-2023·2023-08-23
HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard
Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.
Product
HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8) A2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1084-2023·2023-08-23
Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons
Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.
Product
hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-p
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2412-2023·2023-08-23
Medtronic ventricular catheter system recalled due to incorrect labeling expiration date
Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.
Product
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1086-2023·2023-08-23
Tobramycin Ophthalmic Solution recalled for failed quality specifications
Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.
Product
TOBRAMYCIN OPHTHALMIC SOLUTION — TOBRAMYCIN OPHTHALMIC SOLUTION (TOBRAMYCIN OPHTHALMIC SOLUTION)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1085-2023·2023-08-23
PLUVICTO Injection Recalled for Incorrect Lot and Expiration Date Labels
PLUVICTO (lutetium Lu 177 vipivotide tetraxetan) injection vials were labeled with incorrect lot numbers and expiration dates. The manufacturer is recalling affected lots distributed nationwide.
Product
PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61
Category
Drug
Distribution
Distributed nationwide
CriticalCPSC·23263·2023-08-17
Zipadee Kids Convertible House Bed Frames Recalled for Entrapment and Strangulation Risk
Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds are being recalled due to spindle spacing that can trap a child's torso while preventing their head from passing through, creating a strangulation hazard. At least two children have become entrapped.
Product
Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23783·2023-08-17
Ubio Labs power banks recalled due to fire hazard
Costco is recalling approximately 350,000 Ubio Labs power banks (model PWB1071) that can overheat and ignite. The company has received three fire reports, including one on a commercial flight with four smoke inhalation reports and one minor burn injury.
Product
Ubio Labs power banks
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23782·2023-08-17
Midwest Lubricants Sodium Hydroxide Recalled for Unsafe Packaging
Midwest Lubricants is recalling about 3,000 units of Sodium Hydroxide (Caustic Soda Beads) because the packaging is not child-resistant and the label lacks required hazard information. The product poses a risk of chemical burns and eye irritation.
Product
Midwest Lubricants Sodium Hydroxide
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23265·2023-08-17
Simplay3 Toddler Towers Recalled Due to Fall and Injury Hazards
Simplay3 Toddler Towers can tip over during use, posing fall and injury hazards to young children. The manufacturer has received 16 reports of tipping, including 10 reports of injuries.
Product
Simplay3 Toddler Towers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23262·2023-08-16
Gree Recalls 1.56 Million Dehumidifiers Due to Fire and Burn Hazards
Gree is recalling approximately 1.56 million dehumidifiers sold under brand names including GE, Kenmore, SoleusAir, Seabreeze, and Norpole because they can overheat, smoke, and catch fire, creating fire and burn hazards.
Product
Dehumidifiers
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-1366-2023·2023-08-16
Energy balls recalled for undeclared sesame allergen
Betty Lou's Paleo Java Nuts About Energy Balls are being recalled due to undeclared sesame in the product. The recall affects packages distributed nationwide.
Product
Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds, shelf-stable, 12-month shelf life, 1.5 oz (42g) package and 12/1.5 oz. packages per display box. Packages are sold individually (UPC 0 1607352146 5) or packaged into 12-ct display box (UPC 0 16073
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1401-2023·2023-08-16
Cava Spicy Hummus recalled nationwide for undeclared sesame
Cava Spicy Hummus (8oz, UPC 89832800227) is being recalled because it contains undeclared sesame. The product was distributed nationwide; consumers with sesame allergies may be at risk.
Product
Cava Spicy Hummus UPC 89832800227 Net Wt. 8oz./226.8 g Packaged in clear plastic container. 12 units per case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1421-2023·2023-08-16
Food Recall: ONO Vegan Blueberry Protein Overnight Oats for Undeclared Milk
ONO LLC is recalling ONO Vegan Blueberry Muffin Protein Overnight Oats because they contain undeclared milk, a common allergen. The product was distributed nationwide and poses a risk to consumers with milk allergies.
Product
ONO Vegan Blueberry Muffin Protein Overnight Oats, 2.75oz. UPC 01-95893-47024-2
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2359-2023·2023-08-16
Siemens ARTIS Icono Biplane Angiography Systems Thermal Cable Connector Defect
Siemens recalls ARTIS icono biplane angiography systems with defective cable connectors that may cause thermal overload, burning smell, and loss of imaging functionality during clinical procedures.
Product
ARTIS icono biplane -Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 11327600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2344-2023·2023-08-16
Olympus Endoscope Reprocessor Labeling Revised for Compatibility and Sterilization Parameters
Olympus is revising labeling for its OER-Elite, OER-Pro, and OER-Mini endoscope reprocessors due to incompatible endoscope models and incorrect sterilization parameters in previous labeling. The revisions remove two endoscope models from the compatibility list and correct gas sterilization concentration requirements.
Product
Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2023·2023-08-16
LINK MP Hip Stem trial instruments may require increased removal force during surgery
LINK MP Monoblock hip stem trial instruments may require increased force to remove during surgery, potentially prolonging procedures or requiring surgical modification.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 21 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-121/00
Category
Medical Device
Distribution
Distributed nationwide