State

Missouri product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46601–46625 of 82318

HighFDA (Devices)·Z-2863-2017·2017-08-09
Spectranetics Turbo-Elite Laser Atherectomy Catheters Recalled for Marker Band Risk
Spectranetics is recalling Turbo-Elite Laser Atherectomy Catheters because a marker band may become loose or disengaged when the device is used off-label.
Product
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in the treatment, including atherectomy, of infrainguinal stenosis and occlusions
Category
Medical Device
Distribution
40 states
HighFDA (Devices)·Z-2783-2017·2017-08-09
LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach
LivaNova is recalling Perfusion Tube Sets because the included Medtronic display sets may have pinholes, creating a potential sterile barrier breach.
Product
SORIN GROUP, SMART PERFUSION PACK, LONG PACK, REF 088512600, STERILE EO, Rx Only, 1 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2790-2017·2017-08-09
LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach
LivaNova is recalling Perfusion Tube Sets because the included Medtronic display sets may have pinholes, creating a potential sterile barrier breach.
Product
SORIN GROUP, SMART PERFUSION PACK, SMART 3/16" PEDS PACK, REF 627263601, STERILE EO, Rx Only, 1 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2794-2017·2017-08-09
LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach
LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.
Product
SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8S, REF 044036101, STERILE EO, Rx Only, 1 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2789-2017·2017-08-09
LivaNova Perfusion Tube Sets Recalled for Potential Sterility Breach
LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.
Product
SORIN GROUP, SMART PERFUSION PACK, PUMP AND TABLE PACK, REF 627374101, STERILE EO, Rx Only, 1 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2785-2017·2017-08-09
LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes that compromise sterility.
Product
SORIN GROUP, SMART PERFUSION PACK, SMA PRIMO2X OPTI PACK, REF 088512900, STERILE EO, Rx Only, 1 EA
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1038-2017·2017-08-09
Dr. Reddy's Recalls Pravastatin Sodium Tablets Due to Impurity
Dr. Reddy's Laboratories is recalling specific lots of Pravastatin Sodium tablets because they failed impurity specifications.
Product
PRAVASTATIN SODIUM — PRAVASTATIN SODIUM (PRAVASTATIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2799-2017·2017-08-09
Stryker Neurovascular Recalls Stroke Fast Packs Due to Labeling Mismatch
Stryker Neurovascular is recalling 43 Stroke Fast Packs because the carton sleeve labels did not match the physical contents inside the packs.
Product
Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20, Trevo Pro 14 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK32021001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2803-2017·2017-08-09
Quidel Recalls InflammaDry Sample Collectors Due to Plastic Spurs
Quidel Corporation is recalling InflammaDry sample collectors because in-house testing found plastic spurs at the tips of some units.
Product
InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the visual, qualitative, in vitro detection of elevated levels of the MMP-9 protein in human tears, from patients suspected of having dry eye. InflammaDry is to be used…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1051-2017·2017-08-09
Bayer Recalls Alka-Seltzer Gold Tablets Due to Defective Blister Pack Foil
Bayer HealthCare is recalling Alka-Seltzer Gold effervescent tablets because customer complaints confirmed small holes or cracks in the foil of the blister packs.
Product
Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500041085
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1056-2017·2017-08-09
Teva Recalls Famotidine Tablets Due to Weight Specification Failures
Teva Pharmaceuticals USA is recalling 28,188 bottles of Famotidine 20 mg tablets because they failed tablet weight specifications.
Product
FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2867-2017·2017-08-09
Sentinel CH Recalls MULTIGENT Creatinine Reagents Due to Quality Control Issues
Sentinel CH SPA is recalling MULTIGENT Creatinine (Enzymatic) reagents because Reagent 1 may cause quality control values to shift out of acceptable range.
Product
MULTIGENT Creatinine (Enzymatic), Catalog Numbers 8L24-31 and 8L24-41; IVD. Intended for the quantitative determination of creatinine in human serum, plasma, and urine using the ARCHITECT c Systems The product is a medical device (chemistry reagent) and is intended for the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1042-2017·2017-08-09
Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.
Product
Divalproex Sodium Delayed Release Tablets, USP, 250 mg 100-count bottle (NDC 68382-032-01), b.) 500-count bottle (NDC 68382-032-05),Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2866-2017·2017-08-09
Xintec OptiLITE Laser Surgery Fibers Recalled for Reprocessing Instruction Deficiencies
Xintec Corp is recalling OptiLITE laser surgery products because reprocessing instructions may not meet new standards for cleaning and sterilization.
Product
OptiLITE(TM) Products for Laser Surgery, Catalog Numbers: HTM1020F, HTM1040F, HTM1060F, HTM1010F; Manufactured by CONVERGENT LASTER TECHNOLOGIES The Odyssey 30B is approved for numerous medical procedures. Generally, the primary use of the laser (which includes the fibers)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2802-2017·2017-08-09
Stryker Neurovascular Recalls Stroke Fast Packs Due to Labeling Mismatch
Stryker Neurovascular is recalling 48 Stroke Fast Packs because the pre-printed carton sleeve contents did not match the physical items inside.
Product
Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25, AXS Catalyst 060x132CM - US, EXCELSIOR XT 27 MICROCATHETER, UPN M0033PK62523001 ST 150
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1050-2017·2017-08-09
Bayer Recalls Alka-Seltzer Extra Strength Tablets Due to Defective Packaging
Bayer is recalling Alka-Seltzer Extra Strength effervescent tablets because customer complaints confirmed small holes or cracks in the foil blister packs.
Product
Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500044048
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2801-2017·2017-08-09
Stryker Stroke Fast Pack Recall Due to Mismatched Carton Sleeve Labeling
Stryker Neurovascular is recalling 139 Stroke Fast Packs because the pre-printed contents on the carton sleeve did not match the physical contents of the pack.
Product
Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK43022001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2800-2017·2017-08-09
Stryker Neurovascular Recalls Stroke Fast Packs Due to Labeling Mismatch
Stryker Neurovascular is recalling 63 Stroke Fast Packs because the printed carton contents did not match the physical items inside.
Product
Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1055-2017·2017-08-09
Time-Cap Recalls Ibuprofen Tablets Due to Foreign Capsule Presence
Time-Cap Laboratories is recalling 1,980 bottles of 600 mg ibuprofen tablets because some bottles contained 800 mg tablets.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1041-2017·2017-08-09
Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.
Product
Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054, NDC 68382-031-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1043-2017·2017-08-09
Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.
Product
Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1057-2017·2017-08-09
PD-Rx Pharmaceuticals Recalls Famotidine 20 mg Tablets for Weight Issues
PD-Rx Pharmaceuticals is recalling 100 bottles of Famotidine USP 20 mg tablets because they failed to meet tablet weight specifications.
Product
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1044-2017·2017-08-09
Bayer Recalls Alka-Seltzer Tablets Due to Defective Blister Pack Foil
Bayer HealthCare is recalling Alka-Seltzer Original effervescent tablets because customer complaints confirmed small holes or cracks in the foil of the blister packs.
Product
Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 12-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500040194
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1039-2017·2017-08-09
Teva Recalls Albuterol Sulfate Inhalation Solution Due to Impurities
Teva Pharmaceuticals USA is recalling Albuterol Sulfate Inhalation Solution because high levels of a related compound were detected.
Product
Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials For Inhalation per carton, Rx only, Mfd. for: Watson Laboratories, Inc., Corona, CA 92880; Mfd. by: Cipla Ltd., Verna, Goa INDIA, NDC 0591-3467-53.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V495000·2017-08-08
BMW Recalls 2012-2013 X3 and M6 Models for Air Bag Defect
BMW is recalling 2012-2013 X3 and 2013 M6 vehicles because a defective driver's air bag inflator could cause metal fragments to strike occupants in a crash.
Product
BMW — BMW X3, M6
Category
Vehicle
Distribution
Distributed nationwide