State

Missouri product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48751–48775 of 82325

HighFDA (Devices)·Z-1760-2017·2017-04-19
ConMed Recalls Hyfrecator 2000 Handpiece Sheaths Due to Sterility Labeling Error
ConMed is recalling Hyfrecator 2000 handpiece sheaths because non-sterile units were packaged in pouches labeled as sterile, posing a risk of infection.
Product
HYFRECATOR 2000 HANDPIECE SHEATH, REF/Part Number 7-796-19, Rx ONLY, STERILE, Single Patient Use -- CONMED CORPORATION, 525 FRENCH ROAD UTICA, NY 13502. --- There is no problem with the Hyfrecator 2000 Electrosurgical Units or with cases of P/N 7-796-19 sold in cases as P/N…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1798-2017·2017-04-19
Windstone Medical Setup Packs Recalled for Potential Sterility Compromise
Windstone Medical Packaging is recalling 500 Setup Packs containing Medtronic Curity Eye Pads due to potential sterile packaging compromise.
Product
Setup Pack, part number AMS3112(A Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2017·2017-04-19
Roche Recalls Cobas 8100 Reformatter Modules Due to Rack Crash Risk
Roche Diagnostics is voluntarily recalling 45 Cobas 8100 reformatter modules because a rack crash can cause sample spillage, posing a risk of exposure to infectious material.
Product
Cobas 8100 uni-directional reformatter (BRF) module with Software Version 02-xx
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-1793-2017·2017-04-19
Windstone Medical Minor Operation Kit Recall Due to Sterile Packaging Concerns
Windstone Medical Packaging is recalling 700 Minor Operation Kits because the sterile packaging of the included Medtronic Curity Eye Pad may be compromised.
Product
Minor Operation Kit, part number AMS1530 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1815-2017·2017-04-19
RayStation Radiation Therapy Software Recalled for GPU Driver Error
RaySearch Laboratories is recalling RayStation software due to a potential calculation error in non-standard Citrix environments.
Product
Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1795-2017·2017-04-19
Windstone Medical Recalls Ortho Basic Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 12 Ortho Basic Packs because the sterile packaging of the included eye pads may be compromised.
Product
Ortho Basic Pack, part number AMS6459 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V262000·2017-04-19
Winnebago Recalls 2014-2017 Motorhomes Due to Electrical Interference
Winnebago is recalling 2014-2017 View, VIA, ERA, and Itasca Navion motorhomes because a radio module may interfere with the electrical system, potentially causing engine shutdown or power loss.
Product
WINNEBAGO — WINNEBAGO, ITASCA VIA, VIEW, NAVION, ERA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1786-2017·2017-04-19
Windstone Medical Recalls Custom Kits with Compromised Sterile Eye Pad Packaging
Windstone Medical Packaging is recalling 164 custom kits containing Medtronic Curity Eye Pads due to potential sterile packaging compromise.
Product
Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2017·2017-04-19
ConMed Recalls Hyfrecator 2000 Accessory Packages with Non-Sterile Sheaths
ConMed is recalling Hyfrecator 2000 accessory packages because they contained non-sterile handpiece sheaths labeled as sterile.
Product
Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons , 220 VOLTS AC, REF/Catalog Number 7-900-220, Rx Only, There is no problem with the Hyfrecator 2000 Electrosurgical Units…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1796-2017·2017-04-19
Windstone Medical Packaging Recalls Plastic Packs with Compromised Sterile Eye Pads
Windstone Medical Packaging is recalling 376 plastic kits containing Medtronic Curity Eye Pads because the sterile packaging may be compromised.
Product
Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1783-2017·2017-04-19
Windstone Medical Packaging Recalls Cataract Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 4,065 cataract kits because the sterile packaging of the included eye pads may be compromised.
Product
Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1816-2017·2017-04-19
Hill-Rom TotalCare Bed Systems Recalled for Alarm Malfunction
Hill-Rom is recalling TotalCare Bed Systems because the exit alarm may fail if armed for over 72 hours without triggering.
Product
TotalCare Bed Systems, Model Numbers P1900, PR1900, and U1900 with 3-Level Patient Position Monitoring and Scale Upgrade Kits, Model Numbers P1947A and P1948A).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2017·2017-04-19
Draeger Medical Systems Recalls Delta Patient Monitors Due to Low Oxygen Alarm Failure
Draeger Medical Systems is recalling Delta patient monitors used with Scio gas modules because the low oxygen alarm may fail to sound when oxygen levels drop below the set limit.
Product
Delta, Catalog Number: MS18597 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1800-2017·2017-04-19
Windstone Medical Vitrectomy Packs Recalled for Sterile Packaging Compromise
Windstone Medical Packaging is recalling 100 Vitrectomy Packs because the sterile packaging of the included eye pads may be compromised.
Product
Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2017·2017-04-19
Merge Hemo software recall for incorrect FFR results display
Merge Healthcare is recalling Merge Hemo software versions 9.10.0 through 9.40.0 because they may display incorrect Fractional Flow Reserve values during cardiac catheterization.
Product
Merge Hemo software. The firm name on the labeling is Merge Healthcare, Hartland, WI. Merge Hemo monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1791-2017·2017-04-19
Windstone Medical Eye Pack Recall Due to Sterile Packaging Compromise
Windstone Medical Packaging is recalling 1,330 Eye Packs because the sterile packaging of the included eye pads may be compromised.
Product
Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1788-2017·2017-04-19
Windstone Medical Recalls Dr. Wischmeier Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 1,170 Dr. Wischmeier Packs because the sterile packaging of the included eye pads may be compromised.
Product
Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2017·2017-04-19
BioMerieux Recalls VIDAS Estradiol II Assay Due to Fulvestrant Cross-Reactivity
BioMerieux SA is recalling VIDAS Estradiol II kits because Fulvestrant treatment can cause falsely elevated estradiol results.
Product
VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments of the VIDAS family (VITEK ImmunoDiagnostic Assay System) as an automated quantitative enzyme-linked fluorescent immunoassay (ELFA) to the determination of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1922-2017·2017-04-19
Gerber Pasta Pick-Ups Cheese Ravioli Recalled for Missing Egg Allergen Label
Gerber is recalling Pasta Pick-Ups Cheese Ravioli because the egg allergen is missing from the 'Contains' statement on the packaging.
Product
Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Drained Wt 3 oz (85g) UPC 01500000907-6 , Truncated - written on package as: UPC 159070
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1787-2017·2017-04-19
Windstone Medical Recalls Dicken Eye Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 172 Dicken Eye Packs because the sterile packaging of the eye pads may be compromised.
Product
Dicken Eye Pack, part number CPA-3202-2. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1794-2017·2017-04-19
Windstone Medical Ophthalmic Packs Recalled for Sterile Packaging Compromise
Windstone Medical Packaging is recalling 169 ophthalmic packs containing Medtronic Curity Eye Pads because the sterile packaging may be compromised.
Product
Ophthalmic Pack, Part number WAL1107(A and WAL1190 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1799-2017·2017-04-19
Windstone Medical Vitrectomy Kits Recalled for Sterile Packaging Compromise
Windstone Medical Packaging is recalling Vitrectomy Kits because the sterile packaging of the included Medtronic Curity Eye Pad may be compromised.
Product
Vitrectomy Kit, part number CMP1016(A. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1756-2017·2017-04-19
ConMed Recalls Sterile Handpiece Sheaths Packaged in Error
ConMed is recalling sterile handpiece sheaths that were packaged in error with non-sterile units. The mislabeling could lead to the use of non-sterile sheaths.
Product
Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 100 VOLTS AC, REF/Catalog Number 7-900-100, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Unit. -- ASSEMBLED…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1784-2017·2017-04-19
Windstone Medical Recalls Cataract Kits Due to Sterile Packaging Concerns
Windstone Medical Packaging is recalling 990 cataract kits because the sterile packaging of the included eye pads may be compromised.
Product
Cataract Kit - Dr. Slingsby, part number CMP1017(B. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1759-2017·2017-04-19
ConMed Recalls Sterile Handpiece Sheaths Packaged as Non-Sterile
ConMed is recalling sterile handpiece sheaths that were incorrectly packaged with non-sterile units. This error could lead to the use of non-sterile sheaths in medical procedures.
Product
Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 230 VOLTS AC, REF/Catalog Number 7-900-230, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Units. -- ASSEMBLED…
Category
Medical Device
Distribution
Distributed nationwide