State

Idaho product recalls

20,364 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho specifically in their distribution scope.

About recalls in Idaho

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Idaho consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14876–14900 of 20364

HighFDA (Devices)·Z-0720-2023·2022-12-21
Cordis Angiographic Catheter Extensions Recalled for Male Connector Separation Risk
Cordis angiographic catheter extensions may experience separation at the male connector during use. Approximately 2,915 US units were distributed; users should verify affected lot numbers.
Product
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0514-2023·2022-12-21
ENT Surgical Kits Recalled for Potential Sterility Loss
Stradis Medical is recalling HENRY SCHEIN ENT surgical kits distributed nationwide due to defective outer bag sealing that may compromise sterility. Affected kits were distributed across the US and Canada.
Product
HENRY SCHEIN, ENT SET UP PACK, Item No.570-2742
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2023·2022-12-21
Electrosurgical Suction Coagulator Devices Recalled Due to Potential Suction Port Blockage
ConMed's electrosurgical suction coagulator devices may have blocked suction ports that prevent proper function during procedures. Affected devices could cause procedure delays and require alternative equipment.
Product
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0718-2023·2022-12-21
Siemens allergy test kits recalled for false mold allergen reactivity results
Siemens Healthcare Diagnostics is recalling 560 allergy diagnostic kits (Lot 565) due to potential for falsely elevated mold allergen reactivity, which may result in incorrect test results.
Product
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan Siemens Material Number (SMN): 10711939 For the quantitative measurement of allergen-specific IgE in human serum, as an aid in the clinical diagnosis of IgE mediated allergic disorders.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0516-2023·2022-12-21
Stradis Healthcare Major Extremity Surgical Kits Recalled for Potential Sterility Breach
Stradis Healthcare is recalling Henry Schein Major Extremity surgical kits due to incomplete outer bag sealing that could compromise kit sterility. Affected kits were distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, MAJOR EXTREMITY PACK, Item No.570-2783,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2023·2022-12-21
BBL Chocolate II Agar laboratory culture media recalled for nutrient deficiency
BBL Chocolate II Agar culture media manufactured by Becton Dickinson contains reduced nutrients and may cause false negative results in laboratory bacterial identification testing.
Product
BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0507-2023·2022-12-21
Surgical Procedure Trays Recalled for Potential Sterility Breach
Stradis Medical recalls Henry Schein Basin Pack surgical trays due to potentially incomplete outer packaging seals that may compromise sterility of the medical kits.
Product
HENRY SCHEIN, Basin Pack, Item No.570-1692
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0488-2023·2022-12-21
Stradis Healthcare Oral Surgery Implant Packs Recalled for Incomplete Seal Defect
Stradis Medical recalled 20 oral surgery implant packs with incomplete outer bag sealing that may compromise sterility. Affected lot numbers are 22228490663 and 22242491516, distributed in the US and Canada. No illnesses reported.
Product
STRADIS HEALTHCARE, Basic Implant Pack, Item No.40561BIP, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0529-2023·2022-12-21
Surgical Procedure Kits Recalled Due to Incomplete Outer Bag Sealing
Stradis Healthcare is recalling Henry Schein Custom PK 2 surgical procedure kits due to manufacturing defects that may result in incomplete outer bag sealing, potentially compromising sterility. The recall affects 27 units distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, CUSTOM PK 2, Item No.570-3072
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0515-2023·2022-12-21
Medical and Surgical Procedure Trays Recalled Due to Incomplete Sealing
Stradis Medical is recalling medical and surgical procedure kits with potentially incompletely sealed outer bags that may compromise sterility. Affected healthcare facilities should stop using these kits immediately.
Product
HENRY SCHEIN, OMFS, Item No.570-2779,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0510-2023·2022-12-21
Stradis Medical gynecological surgical kit recalled due to potential sterility breach
Stradis Medical is recalling Henry Schein GYN Pack surgical kits with potentially incompletely sealed outer bags that may compromise sterility. The affected kits were distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, GYN PACK, Item No.570-2625
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2023·2022-12-21
Surgical microscope power supply may overheat and cause unexpected shutdown
Leica Microsystems is recalling 43 Proveo 8 surgical microscopes nationwide due to a potential power supply defect that may cause device overheating and unexpected shutdown during use.
Product
Leica MICROSYSTEMS Proveo 8, Part Number 10449058, surgical microscope system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0506-2023·2022-12-21
General Surgery Procedure Kit Recalled for Sterility Concerns
Stradis Medical is recalling surgical procedure kits with potentially incomplete outer bag seals that may compromise sterility. The recall affects 35 units distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, PROCEDURE KIT, Item No.570-1508, general surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0490-2023·2022-12-21
Surgical Procedure Tray Recall Due to Incomplete Packaging Seal
Stradis Healthcare is recalling oral surgery trays with potentially incompletely sealed packaging that may compromise sterility. No illnesses reported.
Product
STRADIS HEALTHCARE, Surg Pk, Item No.40714IES, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0552-2023·2022-12-21
Surgical Procedure Kits Recalled for Incomplete Outer Bag Seal
Stradis Healthcare is recalling Varicosity Basic Pack surgical procedure kits (105 units) distributed in the US and Canada due to potentially incomplete outer bag sealing that may compromise sterility.
Product
STRADIS HEALTHCARE, Varicosity Basic Pack, Item No.682-947,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0549-2023·2022-12-21
Endovenous Procedure Packs Recalled for Incomplete Bag Sealing
Stradis Healthcare is recalling Endovenous Packs due to incompletely sealed outer bags that may compromise kit sterility. No illnesses have been reported.
Product
www.StradisHealthcare.com, Endovenous Pack, Item No.682-494,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0547-2023·2022-12-21
Stradis Healthcare Medical Vein Kits Recalled for Potential Sterility Breach
Stradis Healthcare is recalling Medical Vein procedure kits due to potentially incomplete sealing of the outer bag that may compromise kit sterility. No illnesses or injuries have been reported.
Product
STRADIS HEALTHCARE, Medical Vein, Item No.682-330,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0555-2023·2022-12-21
Surgical procedure trays recalled due to incomplete outer bag sealing
Stradis Healthcare is recalling surgical procedure trays that may have incompletely sealed outer bags, risking sterility breach. Sixteen units were distributed nationwide and in Canada.
Product
STRADIS HEALTHCARE, Breast, Item No.693-276,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0500-2023·2022-12-21
Stradis Healthcare Introducer Kit Micro recalled for potential sterility compromise
Stradis Healthcare is recalling 180 units of its Introducer Kit Micro cardiovascular devices due to potential incomplete sealing of outer bags that may compromise sterility.
Product
STRADIS HEALTHCARE, Introducer Kit Micro, Item No.525-038, cardiovascular
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0489-2023·2022-12-21
Surgical dental procedure kits recalled due to incomplete bag sealing
Stradis Healthcare is recalling surgical and dental procedure kits due to manufacturing defects that may result in incomplete outer bag sealing and compromised sterility.
Product
STRADIS HEALTHCARE, Surgical Pk, Item No.40649ECS, dental
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0482-2023·2022-12-21
Oral Surgery Tray Kit Recalled for Potential Sterility Breach
ACE Surgical Supply oral surgery tray kits are recalled because the outer packaging may be incompletely sealed, potentially compromising sterility. The kits were distributed throughout the United States and Canada.
Product
ACE Surgical Supply, 17539 CUSTOM KIT STERILE Item No.003-3880, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0542-2023·2022-12-21
Stradis Healthcare surgical procedure kits recalled for incomplete outer bag sealing
Stradis Healthcare has recalled surgical procedure kits due to incomplete outer bag sealing that may compromise sterility. Affected units (40 units, lot 22235489419) were distributed across the United States and Canada.
Product
STRADIS HEALTHCARE, Surgery PK, Item No.682-1728,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0493-2023·2022-12-21
Stradis Healthcare Dental Implant Trays Recalled Due to Incomplete Sealing
Stradis Healthcare is recalling dental implant trays with incomplete outer bag seals that may compromise sterility. Affected units were distributed in the US and Canada.
Product
STRADIS HEALTHCARE, Implants, Item No.41015NSI, dental tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2023·2022-12-21
Single-shot epidural kits recalled due to incomplete outer bag sealing
Stradis Medical is recalling 80 Henry Schein single-shot epidural kits due to potentially incomplete outer bag sealing that could compromise sterility. The recall affects units distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, SINGLE SHOT EPIDURAL, Item No.570-3089
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2023·2022-12-21
Dental Surgical Pack Recalled Due to Incomplete Sterile Seal
Stradis Medical is recalling a dental surgical pack because the outer bag may be incompletely sealed, potentially compromising sterility. Affected units should not be used.
Product
Surgical room, DENTAL SURGICAL PACK, Item No.41236SDSP
Category
Medical Device
Distribution
Distributed nationwide