State

Missouri product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42301–42325 of 82310

HighFDA (Devices)·Z-2241-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 248 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
RECON DRILL 6MM X 439MM; 14-443023 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2243-2018·2018-06-27
C.R. Bard Recalls CritiCore Automated Urine Output and Temperature Monitor
C.R. Bard is recalling CritiCore Automated Urine Output and Temperature Monitors due to measurement errors and undesired alarms.
Product
CritiCore Automated Urine Output and Temperature Monitor
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-2264-2018·2018-06-27
TriMed Recalls Nitinol Surgical Staples Due to Sterilization Record Gaps
TriMed Inc. is recalling 706 units of Nitinol Surgical Staples because quarterly sterilization dose audits could not be verified, posing a potential infection risk.
Product
Nitinol Staple, Elastic Staple Small-Asymmetrical, Sterile R, Model #: a) ES-10x13x15; b) ES-10x16x19; c) ES-10x17x19; d) ES-12x13x15; e) ES-12x15x17; f) ES-12x16x19; g) ES-15x13x16
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-2240-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 304 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
3.2MM X 510MM COCR THD TIP; 14-443053 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0886-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium tablets because they failed impurities and degradation specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0888-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures
Dr. Reddy's Laboratories is recalling 130,081 bottles of Atorvastatin Calcium 40 mg tablets nationwide due to failed impurity and degradation specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2270-2018·2018-06-27
Olympus JF-160F Duodenoscopes Recalled for New Reprocessing Procedures
Olympus Corporation of the Americas is recalling 68 JF-160F duodenoscopes nationwide to implement validated new reprocessing procedures.
Product
Olympus JF-160F duodenoscopes (Model NumberJF-160F)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0878-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Foreign Object
Dr. Reddy's Laboratories is recalling 6,397 bottles of Atorvastatin Calcium 80 mg tablets because a foreign object was found embedded in a tablet.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2261-2018·2018-06-27
Paragon 28 Recalls P28 JAWS Nitinol Staple Kits Due to Missing Drill Guide
Paragon 28, Inc. is recalling P28 JAWS Nitinol Staple System kits because the drill guide is missing from the package.
Product
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones and joints of the foot including fixation of small bone fragments.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0887-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures
Dr. Reddy's Laboratories is recalling specific lots of Atorvastatin Calcium tablets because they failed impurity and degradation specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V433000·2018-06-26
KME Predator Emergency Vehicles Recalled for Lifting Device Defect
KME is recalling 13 Predator emergency vehicles because tip-mounted lifting devices do not meet safety load ratings, posing an injury risk.
Product
KME — KME PREDATOR, PREDATOR SS AERIAL, PREDATOR SS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V432000·2018-06-26
Lexus Recalls Vehicles for Fuel Leak Fire Risk
Toyota is recalling specific Lexus models because fuel pulsation dampers may crack and leak, increasing the risk of a fire.
Product
LEXUS — LEXUS GS 350, IS 350, IS 350C, GS HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18748·2018-06-26
Stanley Workbench LED Light and Power Stations Recalled for Shock Hazards
Baccus Global is recalling Stanley workbench LED light and power stations due to incorrect wiring that poses shock and electrocution hazards.
Product
Stanley workbench LED light and power stations
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18E047000·2018-06-26
Kovatch Tip Mounted Lifting Devices Recalled for Load Rating Defects
Kovatch Mobile Equipment Corp. is recalling certain Tip Mounted Lifting Devices because they do not meet specified load ratings, posing a risk of injury.
Product
EQUIPMENT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18E048000·2018-06-26
TRW Recalls Aftermarket Ball Joints Due to Incorrect Nut Size
TRW is recalling aftermarket replacement Ball Joints with incorrect attachment nut sizes that may cause loss of steering control.
Product
STEERING recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18181·2018-06-26
Huish Outdoors Recalls Scuba Diving Regulators Due to Drowning Hazard
Huish Outdoors is recalling Oceanic and Hollis scuba diving regulators because they can restrict airflow at low tank pressures, posing a drowning hazard to divers.
Product
Oceanic and Hollis scuba diving regulators
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V428000·2018-06-25
Forest River Recalls 2019 Wildwood and Salem Trailers for Wiring Defect
Forest River is recalling 2019 Wildwood and Salem trailers because a wiring defect may prevent brakes from engaging if the trailer detaches.
Product
FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V430000·2018-06-25
Audi Recalls 2013-2015 S8 and A8 Models for Fuel Leak Risk
Volkswagen Group of America is recalling 2013-2015 Audi S8 and A8 vehicles because a fuel supply line may leak, increasing fire risk.
Product
AUDI — AUDI A8, S8
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V429000·2018-06-25
Keystone Recalls 2019 Summerland Trailers Due to Incorrect Tire Label
Keystone is recalling 2019 Summerland recreational trailers because the Federal Identification Label lists an incorrect tire rim size, which could lead to improper rim replacement.
Product
KEYSTONE — KEYSTONE SUMMERLAND
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V424000·2018-06-25
Spartan Emergency Vehicles Recalled for Fire Pump Solenoid Corrosion
Spartan Motors is recalling 2009-2018 Gladiator and MetroStar emergency vehicles because internal corrosion in the fire water pump solenoid may cause loss of water pressure, increasing injury risk.
Product
SPARTAN — SPARTAN METROSTAR, GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V426000·2018-06-25
Mazda Recalls 2018 CX-5 Vehicles for Side Air Bag Deployment Defect
Mazda is recalling 2018 CX-5 vehicles because side curtain air bags may not unfold properly in a crash, increasing injury risk.
Product
MAZDA — MAZDA CX-5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V427000·2018-06-22
Audi Recalls A4, A6, and RS4 Models Due to Air Bag Inflator Defect
Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
AUDI — AUDI A4, A6, RS 4, RS4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V425000·2018-06-21
REV Recalls 2019 Fleetwood and Holiday Rambler Motorhomes for Wiring Fire Risk
REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because non-flexible wiring in the bedroom slide-out may damage and cause a fire.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V423000·2018-06-21
E-One Recalls 2016-2017 Cyclone II Emergency Vehicles Due to Ladder Fracture Risk
E-One is recalling 2016-2017 Cyclone II emergency vehicles because stress fractures in the aerial ladder tubing could cause failure and injure the bucket occupant.
Product
E-ONE — E-ONE CYCLONE II
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V422000·2018-06-21
Triple E RV Recalls 2017-2018 Wonder Models Due to Wiring Defect
Triple E RV is recalling 2017-2018 Wonder recreational vehicles because water can corrode wiring in the trailer tow module, potentially causing electrical shorts, fire, or crash risks.
Product
TRIPLE E RV — TRIPLE E RV WONDER
Category
Vehicle
Distribution
Distributed nationwide