All recall categories

Recalls distributed in Missouri

These notices name Missouri in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,082 stored notices name Missouri, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Missouri too — those are in the archive.

Medical devices

Reported Jul 11, 2018

Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Terumo Medical Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2018

Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Trilliant Surgical Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2018

Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Absonutrix

FDA (openFDA food enforcement)

Medical devices

Reported Jul 4, 2018

Amalgatome SD, COAXIAL PNEUMATIC HOSE, SCHRADER, Model X101004

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Exsurco Medical

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2018

Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Golden Star Wholesale Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 4, 2018

Single Chamber Temporary External Pacemaker, Model 53401

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 4, 2018

Brilliance Big Bore Radiology 728244

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 4, 2018

RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jul 4, 2018

Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2018

Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Utz Quality Food Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2018

CritiCore Automated Urine Output and Temperature Monitor

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

VNS Therapy Programmer, Model 3000, v1.0 System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cyberonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Draeger Medical, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 27, 2018

Kellogg's Honey Smacks, 15.3 oz. and 23 oz.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Kellogg Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2018

P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Paragon 28, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

Nitinol Staple, Elastic Staple Large-Asymmetrical, Sterile R, Model #: a) ES-18x15x17; b) ES-18x17x19

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

TriMed Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Angiodynamics Inc. (Navilyst Medical Inc.)

37 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2018

Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

New Century Snacks LLC

FDA (openFDA food enforcement)

Food

Reported Jun 20, 2018

Commercial breaders and batters Product B58042 Breader XI- 50 pound bags Product B58915 Breader X1- 40 pound bags…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Newly Weds Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

Part #: SAM XT-M, Model: Tactical Black or Military

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Seaberg Company Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Priano Rosso Pesto Sauce, 6.7oz glass jar

High riskUsing this product could cause serious injury, illness or death — stop using it now.

BLM Products U. Vertriebsges

FDA (openFDA food enforcement)

Food

Reported Jun 13, 2018

Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic package with UPC 4770049011188.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Desly International Corp.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.