Recalls distributed in Kansas
These notices name Kansas 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.
2,889 stored notices name Kansas, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Kansas too — those are in the archive.
Reported Sep 16, 2026Updated Sep 22, 2026
HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 16, 2026Updated Sep 29, 2026
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medical Action Industries, Inc. 306
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
20 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961
High riskUsing this product could cause serious injury, illness or death — stop using it now.Botticelli Foods, LLC
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 13, 2026
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Byron White Formulas, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyer's Grand Ice Cream Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 16, 2026
Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyer's Grand Ice Cream Inc.
3 more products in this recall
FDA (weekly enforcement report)
Reported Sep 2, 2026Updated Sep 7, 2026
FUJIFILM Synapse PACS software v7.4.310; radiological image processing system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FUJIFILM Healthcare Americas Corporation
FDA (openFDA device enforcement)
Reported Sep 2, 2026Updated Sep 16, 2026
IV Sets with drip chambers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (weekly enforcement report)
Reported Sep 2, 2026Updated Sep 7, 2026
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LLC
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kico Knee Innovation Company
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Prospector Popcorn, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Dentsply Sirona Capsule Mixer Model No. 5546068
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SDI Limited
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 7, 2026
Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.529 Commerce, LLC
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 7, 2026
ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe USA Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OBP Medical Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
GM Helix Implant, Endosseous Dental Implant Article No. 109.984
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
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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.