State

Idaho product recalls

72,907 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total: 3,517
Critical: 364
Severe: 1,023
Most recent: 2026-09-06

Of the 3,517 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,023 (29%) are Severe.

Which agencies issued them

These figures cover only the 3,517 recalls whose distribution notice names Idaho specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1301–1325 of 76424

SevereFDA (Drugs)·D-0620-2026·2026-06-17
Beekeeper's Naturals saline nasal spray recalled for microbial contamination
Beekeeper's Naturals Saline Nasal Spray with propolis and xylitol, 1 fl oz, is being recalled for microbial contamination of non-sterile products. 1,680 bottles are affected.
Product
BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91789.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0942-2026·2026-06-17
Moringa green superfood capsules may be contaminated with Salmonella
TNVitamins and Doctor's Pride moringa green superfood capsules are being recalled because the product may be contaminated with Salmonella. 13,000 bottles are affected.
Product
1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules)
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2337-2026·2026-06-17
CORFLO Safety PEG kit 50-4320 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2026·2026-06-17
Plum Duo infusion pumps may not display soft limit alerts
Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Product
Plum Duo Infusion Pump, 40002-0401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2335-2026·2026-06-17
CORFLO Safety PEG kit 30-6312 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.
Product
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2342-2026·2026-06-17
MIC Safety 20 Fr push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 20 Fr PUSH OTW, catalog number 7170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 901 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2398-2026·2026-06-17
Siemens Dimension tacrolimus reagent cartridges may bias results positively
Three lots of the Siemens Dimension Tacrolimus Flex reagent cartridge are being recalled because of a potential positive bias in quality control and patient sample results.
Product
Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2409-2026·2026-06-17
Halyard drape packs shipped without undergoing validated sterilization process
Halyard Drape Packs, kit code LMDP36-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 72 kits affected.
Product
Halyard, Drape Pack. Kit Code: LMDP36-01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2348-2026·2026-06-17
MIC Safety 20 Fr push OTW PEG kits contain recalled lidocaine
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PUSH OTW, catalog number 8170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0607-2026·2026-06-17
Budesonide inhalation ampules contain black and brown specks and particles
Budesonide Inhalation Suspension, 1 mg/2 mL single-dose ampules from Sun Pharmaceutical, is being recalled after a quality complaint of black or brown specs and particles in the solution.
Product
BUDESONIDE — BUDESONIDE (BUDESONIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2413-2026·2026-06-17
Orca single use endoscope valves recalled over sticking suction buttons
Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.
Product
Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2351-2026·2026-06-17
MIC Safety 20 Fr PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues. 6,005 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2406-2026·2026-06-17
MOSAIQ oncology software may fail to load adapted treatment plan
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
Product
MOSAIQ Oncology Information System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2318-2026·2026-06-17
GE Allia Moveo angiographic systems pose shock risk to service personnel
Allia Moveo angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Three units affected.
Product
Allia Moveo angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2399-2026·2026-06-17
Hintermann left talar implant packaging contained a right-side device
Hintermann Series Talar Implants, Left, Size 2, are being recalled because packaging and labeling for a left implant contained a right implant device. 67 units are affected.
Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2361-2026·2026-06-17
Medartis APTUS compression screws have off-centre cannulation in affected lots
Medartis APTUS 5.0 headed cannulated compression screws for bone fixation are being recalled because the cannulation of the screw is not centered. 13 units are affected.
Product
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2026·2026-06-17
MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2316-2026·2026-06-17
GE Allia IGS 7 Pulse systems pose shock risk to servicers
Allia IGS 7 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 35 units affected.
Product
Allia IGS 7 Pulse angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2322-2026·2026-06-17
TDC VELOCE 23 gauge vitrectomy cutters may have loose outer knife
TDC VELOCE 23G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
Product
TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2336-2026·2026-06-17
CORFLO Safety PEG kit 30-6316 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 41 kits are affected.
Product
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2407-2026·2026-06-17
Halyard pain packs shipped without validated sterilization in Iowa
Halyard Pain Packs, kit code AMPK48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 120 kits affected.
Product
Halyard, Pain Pack. Kit Code: AMPK48-01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2321-2026·2026-06-17
Bicarby dialysate luer-lock connections may leak fluid onto floors
Bicarby Dialysate across six model numbers is being recalled because luer-lock leaks during preparation present a potential slip and fall hazard from fluid on the floor.
Product
Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2347-2026·2026-06-17
MIC Safety 14 Fr push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 14 Fr PUSH OTW, catalog number 8170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2026·2026-06-17
Abbott Merlin pacemaker programmer may fail to terminate threshold test
Merlin Patient Care System programmer software is being recalled because a malfunction during a pacing capture threshold test may stop the command to terminate the test being communicated.
Product
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2340-2026·2026-06-17
CORFLO Safety PEG kit 50-6316 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 54 kits affected.
Product
Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide