State

Missouri product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52451–52475 of 82328

HighFDA (Devices)·Z-2689-2016·2016-09-07
Mindray A7 Anesthesia Delivery System Recalled for Potential Oxygen Leak
Mindray is recalling 167 A7 Anesthesia Delivery Systems due to a potential leak on the back-up oxygen and air cylinder yokes.
Product
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1994-2016·2016-09-07
Tippin's Key Lime Pie Bases Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 8-inch Key Lime Pie Bases because they may contain low levels of peanut residue. The product was distributed to seven states.
Product
Tippins 8" Key Lime Base packaged in ?. UPC code is 680816001851. Packaged in 12 pie bases per case. Shipped frozen. Net wt. 21oz each.
Category
Food
Distribution
7 states
HighNHTSA·16C007000·2016-09-07
Evenflo Recalls Evolve 3-in-1 Booster Seats Due to Harness Loosening Risk
Evenflo is recalling specific Evolve 3-in-1 Combination Booster Seats because children can access a button to loosen the harness, increasing injury risk in a crash.
Product
CHILD SEAT:HARNESS:STRAP/WEBBING recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2670-2016·2016-09-07
Philips Recalls UNIQ 1.0 Fluoroscopy Systems Due to Power Supply Failures
Philips is recalling 1,536 UNIQ 1.0 fluoroscopy systems because certain low-voltage DC power supplies have an increased failure rate.
Product
UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; UNIQ FD10 OR Table, 722033; UNIQ FD10/10 OR Table, 722034; UNIQ FD20 OR Table, 722035; UNIQ FD20/20, 722038; UNIQ FD20/20 biplane OR Table, 722039; UNIQ FD20/15, 722058…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1993-2016·2016-09-07
Tippin's Keylime Pie Bases Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 60 cases of 9-inch Keylime Pie Bases because they may contain low levels of peanut residue.
Product
Tippins 9" Keylime Base packaged in ?. UPC code is 680816000205. Packaged in 18 pie bases per case. Shipped frozen. Net wt. 31oz each.
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2672-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 30,719 diamond coated tips and burs because labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the Ultrasonic Scaler (VARIOS 350 LUX, VARIOS 350, VARIOS 150 LUX, VARIOS 150). The intended use of the tips is based on the parent device. For the ultrasonic scalers and the sonic air scaler, the tips are used for various…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2687-2016·2016-09-07
Baxter Non-DEHP Micro-Volume Extension Set Recalled for Sterility Compromise
Baxter Healthcare is recalling 15,257 units of Non-DEHP Micro-Volume Extension Sets because improper sealing compromised product sterility.
Product
Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single use nonpyrogenic fluid pathway; 50 sets per case; For the administration of drugs and solutions to a patient's vascular system through a vascular access…
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-2674-2016·2016-09-07
Nakanishi Diamond Coated Dental Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 4,284 diamond coated dental tips because the packaging failed to indicate they are single-use only, posing a risk of cross-contamination.
Product
Diamond Coated Tips and Burs are accessories to the air powered dental handpiece (S-MAX pico) The intended use of the tips is based on the parent device. For burs used with the dental handpieces, the intended use is general dental actions such as removing carious material…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2712-2016·2016-09-07
Elekta Monaco RTP System Software Recall for Contour Deletion Error
Elekta, Inc. is recalling the Monaco RTP System software due to a defect where deleted contours may remain in treatment plans.
Product
Monaco RTP System Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Category
Medical Device
Distribution
40 states
HighFDA (Food)·F-1995-2016·2016-09-07
Tippin's Mini Key Lime Pie Bases Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 32 cases of Mini Key Lime Pie Bases because they were manufactured with an ingredient that may contain low levels of peanut residue.
Product
Tippins Mini Key Lime Base packaged in ?. UPC code is 680816000106. Packaged in 30 pie bases per case. Shipped frozen. Net wt. 11oz each.
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2669-2016·2016-09-07
Philips Recalls Allura Xper Systems Due to Power Supply Failure Risk
Philips is recalling 1,536 Allura Xper medical imaging systems because certain low-voltage DC power supplies have an increased failure rate.
Product
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura Xper FD20/10 biplane, 722029; Allura Xper FD10 OR Table, 722033; Allura Xper FD10/10 OR Table, 722034; Allura Xper FD20 OR Table, 722035; Allure Xper…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1991-2016·2016-09-07
Tippin's Key Lime Pie Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 8-inch Key Lime Pies because an ingredient may contain low levels of peanut residue.
Product
Tippins 8" Key Lime Pie packaged in aluminum pie plates with plastic covers. The responsible firm listed on the label is TGP, LLC Kansas City, KS 66106. UPC code is 680816050057. Packaged in 8 pies per case. Shipped frozen.
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-1474-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47477-5, Shade 02 (VF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2706-2016·2016-09-07
Terumo Cardiovascular Procedure Kits Recalled for Incorrect Tubing Coating Labeling
Terumo is recalling 2,207 cardiovascular procedure kits because they are labeled as containing coated tubing but actually contain non-coated tubing.
Product
Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled containing Coated Tubing as follows: This product is intended for use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it. This product is a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1475-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47478-2, Shade 03 (MF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1477-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1478-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48241-1, Shade 06 (D-G)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2711-2016·2016-09-07
Nidek Specular Microscope CEM-530 Software Recall for Unapproved Feature
Nidek Inc is recalling 29 Specular Microscope CEM-530 units because software versions 1.08 and 1.09 include an unapproved analysis feature.
Product
SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Microscope CEM-530 provides non-contact, high magnification image capture of endothelium enabling observation of the size and shape of cells. Information such as the number of…
Category
Medical Device
Distribution
18 states
LowFDA (Drugs)·D-1473-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47476-8, Shade 01 (VF-N)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1476-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47479-9, Shade 04 (M-N)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V640000·2016-09-06
Acura Recalls 2015 TLX Vehicles for Transmission Wire Harness Defect
Honda is recalling 2015 Acura TLX vehicles because transmission wire harness connections may have insufficient crimps, causing the vehicle to unexpectedly shift to neutral and increasing crash risk.
Product
ACURA — ACURA TLX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V641000·2016-09-06
Audi Recalls 2017 Q7 Vehicles for Third-Row Seat Back Defect
Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the third-row seat back may move forward in a crash, increasing injury risk.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V643000·2016-09-06
Ford Recalls Multiple Models Due to Door Latch Defect
Ford is recalling specific 2012-2016 vehicles because door latches may break, allowing doors to open while driving.
Product
FORD — FORD, LINCOLN MUSTANG, ESCAPE, TRANSIT CONNECT, MKC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V644000·2016-09-06
Mazda Recalls Vehicles Due to Corroded Lift Gate Support Struts
Mazda is recalling specific 2010-2016 models because lift gate support struts may corrode and break, causing the gate to drop unexpectedly and injure users.
Product
MAZDA — MAZDA MAZDASPEED3, MAZDA3, MAZDA5, CX-5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V642000·2016-09-06
Audi Recalls Vehicles Due to Inoperative Side Marker Lights
Volkswagen Group of America is recalling certain Audi models because software may cause side marker lights to fail, reducing visibility at night.
Product
AUDI — AUDI A4 ALLROAD, TT ROADSTER, A3 CABRIOLET, Q3
Category
Vehicle
Distribution
Distributed nationwide