State

Idaho product recalls

73,096 recalls have nationwide distribution and so reach Idaho. 3,520 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total: 3,520
Critical: 364
Severe: 1,025
Most recent: 2026-09-23

Of the 3,520 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 1,025 (29%) are Severe.

Which agencies issued them

These figures cover only the 3,520 recalls whose distribution notice names Idaho specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8601–8625 of 76616

SevereFDA (Devices)·Z-0654-2025·2024-12-25
Kirwan Surgical Disposable Bipolar Pencils recalled for potential tube failure
Kirwan Surgical Products is recalling 80,060 Disposable Bipolar Pencils (Model 14-5011) because the outer stainless-steel tube may break or detach during surgical use. The devices were distributed worldwide.
Product
Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil, straight. Model/Catalog Number: 14-5011 The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0658-2025·2024-12-25
Walcott Bipolar Pencil Surgical Instrument Recalled for Potential Tube Detachment
Kirwan Surgical Products is recalling Walcott Bipolar Pencil 25 Gauge surgical instruments due to potential breakage or detachment of the stainless-steel tube. The affected pencils are used in eye and soft tissue surgery.
Product
Walcott Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: RX14-5011. Product Description: The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization of the re
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0661-2025·2024-12-25
Medtronic Becker Neurosurgical Drainage Systems Recalled for Cracked and Leaking Stopcocks
Medtronic Neurosurgery recalls Becker External Drainage and Monitoring Systems due to reports of cracks and leaks in stopcocks. The recalled systems are used to drain cerebrospinal fluid and monitor pressure in neurosurgery patients.
Product
Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER NO Y-SITE 25120 EDMS II 25120 BECKER W/1-WAY VALVE 26040 KIT 26040 BECKER EDMS II 27609 BECKER 27609 W/NEEDLESLESS INJ. SITE 27670 BECKER 27670 STOP BELOW DC NDL-LS IN 27672 BECKER 27672 ONEWAY VLV Y-SI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0656-2025·2024-12-25
Surgical Bipolar Pencil Recall: Risk of Tube Breakage During Eye Surgery
Kirwan Surgical Products is recalling disposable bipolar surgical pencils used in eye surgery because the outer stainless-steel tube may break or detach during use.
Product
Accutome/Microsurgical Disposable Bipolar Pencil 5 in. (12.7cm) 25 Gauge Straight. Model/Catalog Number: AB-7004 The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauter
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0655-2025·2024-12-25
Kirwan Surgical Bipolar Pencil Recalled Due to Potential Tube Breakage
Kirwan Surgical Products is recalling its Disposable 25-gauge Bipolar Pencil (Model 14-5011L) because the outer stainless-steel tube may break or detach during use. The defect could create a safety hazard during eye surgery and other soft tissue procedures.
Product
Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil, straight, Long. Model/Catalog Number: 14-5011L The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauteri
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0688-2025·2024-12-25
K-Systems G85 Mini Incubator May Exceed Desired Temperature
CooperSurgical recalls 37 K-Systems G85 Mini Incubators because the device warming surfaces may exceed the desired set temperature. The unit alarms when this occurs, but affected serial numbers require verification.
Product
Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-0693-2025·2024-12-25
Bronchoscopic system may lose power due to defective component
A defective power component in Noah Medical's Galaxy System bronchoscope may cause sudden power loss during procedures, potentially leading to lung injury or pneumotharax.
Product
Galaxy System (GAL-001)
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0706-2025·2024-12-25
GE OEC 9800 X-Ray System Recalled for Insufficient Tube Sealing
GE OEC 9800 fluoroscopic X-ray systems are recalled due to insufficient sealing of X-ray tubes, which can result in oil leaks and loss of imaging capability. 25 systems distributed in the U.S. and internationally are affected.
Product
OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscop
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0704-2025·2024-12-25
Fluoroscopic X-Ray System Recalled for Insufficient X-Ray Tube Sealing
GE OEC Elite mobile fluoroscopic X-ray systems are recalled due to insufficient sealing of X-ray tubes, which can cause oil leaks and loss of imaging capability. Approximately 100 systems have been affected.
Product
OEC Elite REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical
Category
Medical Device
Distribution
45 states
HighFDA (Drugs)·D-0152-2025·2024-12-25
Ophthalmic solution recalled for lack of sterility assurance
Regener-Eyes ophthalmic solution is being recalled due to lack of sterility assurance. Approximately 170,812 bottles distributed nationwide are affected.
Product
LITE Regener-Eyes, Ophthalmic Solution (glycerin 0.4%), 3mL bottles, Distributed by: Regener-Eyes, Tampa, FL; Manufactured by: Regenerative Processing Plant, LLC, 34176 US HWY 19N, FL, NDC 82305-006-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0703-2025·2024-12-25
OEC 3D Mobile Fluoroscopic X-Ray System Tube Sealing Defect Recall
GE OEC Medical Systems is recalling 84 OEC 3D mobile fluoroscopic X-ray systems due to manufacturing defects in X-ray tube sealing that can cause oil leaks and loss of imaging capability.
Product
OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging system used to assist trained surgeons and other qualified physicians. The system is used to provide fluoroscopic Xray images and volumetric reconstructions durin
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0709-2025·2024-12-25
Medical Imaging Software Recall: mint Lesion Orientation Display Malfunction
Mint Medical is recalling mint Lesion software versions 3.9.0–3.9.5 due to a malfunction that may display incorrect orientation labels for certain medical images. 65 units were distributed in the US and internationally.
Product
mint Lesion, Software Versions: 3.9.0 through 3.9.5.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0692-2025·2024-12-25
K-Systems Incubator Device Recall: Temperature May Exceed Desired Setting
CooperSurgical is recalling 34 K-Systems incubator devices used in assisted reproduction procedures. The warming surfaces may exceed the desired set temperature, though the device will alarm if this occurs.
Product
Brand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number: Multiple/unknown Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g.,
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-0657-2025·2024-12-25
Ambler Surgical Bipolar Pencil recalled for outer tube structural failure
Kirwan Surgical Products is recalling the Ambler Surgical Bipolar Pencil 25 Gauge Straight (Model PD7226) because the outer stainless-steel tube may break or detach during use. 4,470 units worldwide are affected.
Product
Ambler Surgical Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: PD7226. The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization of the retinal area durin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0142-2025·2024-12-25
FDA Recalls Health-Tec Benzocaine Topical Anesthetic Due to Manufacturing Defect
Keystone Industries recalls Health-Tec Topical Anesthetic (Benzocaine 20%) lot BNZ-001646 due to manufacturing defects. Scratches found in the mixing vessel caused product rejection designation, but product was inadvertently shipped.
Product
HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0284-2025·2024-12-25
Impossible Savory Ground Sausage Recalled Due to Potential Metal Contamination
Impossible Foods is recalling Impossible Savory Ground Sausage nationwide due to potential metal contamination. Consumers should not consume affected products and should return them to their retailer.
Product
Impossible Savory Ground Sausage Meat from plants 14oz chub, UPC 8 16697 02108 8; 8 retail chubs per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0140-2025·2024-12-25
Dental City Topical Anesthetic Gel Recalled Due to Manufacturing Defect
Dental City Topical Anesthetic Gel (Benzocaine 20%) is recalled because the product was released and distributed despite failing quality inspection. Scratches were found in the mixing vessel during routine inspection.
Product
Dental City, Topical Anesthetic Gel, Benzocaine 20%, Net Content: 1 oz. (30 ml), Gluten Free, Manufactured for: Dental City, Green Bay, WI 54311, dentalcity.com.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0139-2025·2024-12-25
Primo Topical Anesthetic Gel Recalled for Manufacturing Defect
Primo Topical Anesthetic Gel (Benzocaine 20%) is recalled due to manufacturing defect. A Quality Unit inspection found scratches in the mixing vessel, causing inadvertent release of product that should have been rejected.
Product
Primo, Topical Anesthetic gel, Benzocaine 20%, Net Content: 1 oz. (30g), Gluten Free, Manufactured for: Primo Dental Products, 845 Third Avenue, 6th Floor, New York, NY 10022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0705-2025·2024-12-25
OEC 9900 Mobile Fluoroscopic X-Ray System Recall for Sealing Defect
GE OEC Medical Systems is recalling 78 OEC 9900 Elite mobile fluoroscopy systems due to insufficient sealing of X-ray tubes. The defect can result in oil leaks and loss of fluoroscopic imaging capability.
Product
OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedures. Examples of clinical application ma
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0710-2025·2024-12-25
Medical imaging software recall for incorrect DICOM orientation labels
Mint Lesion software versions 3.10.0 and 3.10.1 may display incorrect orientation labels for certain DICOM medical images. The defect affects 18 units distributed across the US and internationally.
Product
mint Lesion, Software Versions: 3.10.0 and 3.10.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0687-2025·2024-12-25
K-Systems G73 Dry Bath Incubator may exceed target temperature
CooperSurgical is recalling K-Systems G73 Dry Bath Incubators because warming surfaces may exceed the desired set temperature. The device alarms when this occurs.
Product
Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and embryos), at c
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-0690-2025·2024-12-25
K-Systems T47 Warming Plate May Exceed Set Temperatures
CooperSurgical recalls K-Systems T47 Warming Plates because temperature may exceed the desired set value, potentially affecting biological materials. The device alarms appropriately when this occurs.
Product
Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23055 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes
Category
Medical Device
Distribution
14 states
HighFDA (Drugs)·D-0151-2025·2024-12-25
VCF Contraceptive Pre-filled Applicators Recalled for Out-of-Specification Active Ingredient
Apothecus Pharmaceutical recalls 33,659 boxes of VCF nonoxynol-9 contraceptive gel nationwide due to out-of-specification active ingredient assay from manufacturing deviations. No illnesses reported.
Product
VCF CONTRACEPTIVE PRE-FILLED APPLICATORS — VCF CONTRACEPTIVE PRE-FILLED APPLICATORS (NONOXYNOL-9)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0292-2025·2024-12-25
Whole Foods Organic Carrots & Celery Recalled Due to E. coli O121:H19 Contamination Risk
F&S Fresh Foods is recalling Whole Foods Market Organic Carrots & Celery due to potential E. coli O121:H19 contamination. The affected products were distributed in AZ, CA, HI, ID, and NV.
Product
WHOLE FOODS MARKET, Organic Carrots & Celery, NET WT. 15 oz (425 g), PERISHABLE KEEP REFRIGERATED, Packed For: Whole Foods Market Austin, TX 78703, Pre-washed and ready to eat
Category
Food
Distribution
5 states
HighFDA (Drugs)·D-0146-2025·2024-12-25
Quala Dental Topical Anesthetic Gel Recalled for Manufacturing Equipment Defect
Quala Dental Products topical anesthetic gel (20% benzocaine) is recalled due to manufacturing equipment defects. The bulk product was inadvertently released despite Quality Unit rejection after inspection found scratches on the mixing vessel.
Product
Quala Dental Products, Topical Anesthetic Gel, Contains 20% Benzocaine, Net Contents: 1 oz (30g), Gluten Free, Quala Dental Products, Made in USA for: NDC, Inc, 407 New Sanford Road, La Vergne, TN 37086, www.quala.com
Category
Drug
Distribution
Distributed nationwide