All recall categories

Recalls distributed in Idaho

These notices name Idaho 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.

2,107 stored notices name Idaho, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Idaho too — those are in the archive.

Medical devices

Reported Sep 23, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

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

Bard Access Systems, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

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

Bd Switzerland Sarl

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

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

Happiest Baby, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Plum administration sets

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

ICU Medical, Inc.

7 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Philips Patient Information Center iX REF:866389

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

Philips North America

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 16, 2026

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…

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

C.R. Bard Inc.

5 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 16, 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 (weekly enforcement report)

Food

Reported Sep 10, 2026

Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Evergreen Fresh Sprouts LLC

FDA (recalls & safety alerts)

Medical devices

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

19 more products in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Meat & poultry

Reported Sep 6, 2026Updated Sep 17, 2026

Prime Line Distributors, Inc. and Ferrarini USA, Inc. Recall Imported Ready-To-Eat Pork Guanciale Products Due to…

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

Recalling firm not stated

USDA FSIS

Food

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)

Food

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)

Food

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)

Food

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)

Drugs

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

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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.