State

Idaho product recalls

73,381 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: 1,217
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 1,217 (35%) are Severe.

Which agencies issued them

These figures cover only the 3,520 recalls whose distribution notice names Idaho specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18776–18800 of 76901

HighFDA (Devices)·Z-0559-2023·2022-12-21
NUVASIVE MAGEC 2 Rod Spinal Bracing System Recalled for Sterile Packaging Failure
NuVasive is recalling the MAGEC 2 Rod spinal bracing system due to potential failure of the sterile packaging barrier, which could compromise device sterility.
Product
NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of scoliosis. REF Model Numbers/NSO Item #/Product Description MC2-4590S / PA0684-001 / MAGEC 2 Rod, 4.5mm 90mm Standard MC2-5590S / PA0684-002 / MAGEC 2…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0491-2023·2022-12-21
Stradis Healthcare Oral Surgery Trays Recalled Due to Incomplete Sealing
Stradis Healthcare is recalling oral surgery trays due to incomplete outer bag sealing that may compromise the sterility of the surgical kit.
Product
STRADIS HEALTHCARE, pack Item No.40788SMS, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0484-2023·2022-12-21
BASIC IMPLANT PACK Recalled for Incomplete Outer Bag Sealing
Stradis Medical is recalling the BASIC IMPLANT PACK (Item 40310SBI) due to incomplete outer bag sealing that may compromise sterility. 80 units were distributed nationwide and in Canada.
Product
BASIC IMPLANT PACK, Item No. 40310SBI, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0523-2023·2022-12-21
Procedure Trays Recalled for Potential Sterility Breach Due to Incomplete Sealing
Stradis Medical recalls Henry Schein procedure trays because the outer bag may be incompletely sealed, risking sterility breach. The trays were distributed nationwide and in Canada.
Product
HENRY SCHEIN, PROCEDURE TRAY, Item No.570-2900,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0520-2023·2022-12-21
Medical procedure trays recalled for incomplete outer bag sealing
Stradis Medical recalls Henry Schein temp stimulator supplies due to incomplete outer bag sealing that may compromise kit sterility. Affected units should not be used until reviewed.
Product
HENRY SCHEIN, TEMP STIMULATOR SUPPLIES, Item No.570-2883
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0539-2023·2022-12-21
Stradis Ablation Pack Recalled for Potentially Compromised Sterile Seal
Stradis Healthcare is recalling Ablation Pack Item No. 682-130 due to incomplete outer bag seals that may compromise sterility. The defect may allow contamination of surgical kits.
Product
STRADIS HEALTHCARE, Ablation Pack, Item No.682-130,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0524-2023·2022-12-21
Stradis Healthcare Surgical Knee Packs Recalled for Incomplete Sealing
HENRY SCHEIN Knee Packs are being recalled due to incomplete outer bag sealing that may breach sterility. Affected surgical kits were distributed in the US and Canada.
Product
HENRY SCHEIN, Knee Pack, Item No.570-2908,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2023·2022-12-21
Henry Schein Universal Tray Recall for Incomplete Sealing
Stradis Medical recalls 675 Henry Schein Universal Trays due to incomplete outer bag sealing that may compromise sterility. The defect affects surgical procedures nationwide and in Canada.
Product
HENRY SCHEIN, UNIVERSAL TRAY, Item No.570-2787
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0512-2023·2022-12-21
Medical and Surgical Procedure Trays Recalled for Incomplete Seal
Stradis Medical recalled Henry Schein Basic Pack medical and surgical procedure trays due to manufacturing defects causing incomplete outer bag seals that may compromise sterility. The affected kits were distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, BASIC PACK, Item No.570-2719, UDI/DI (case) H65857027191, UDI/DI (kit)M75257027190, Serial/Lot Numbers: 22242489505
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2023·2022-12-21
Linear accelerator software addresses potential wrong-site treatment risk
Siemens linear accelerator systems may allow users to select the wrong treatment site, potentially delivering radiation to the wrong location. The FDA classified this Class II recall affecting 8 units across seven U.S. states.
Product
ARTISTE, ONCOR and PRIMUS with syngo RT Therapist with software version 4.3.1 MR3. Material Number: 8162815 Intended Use: Family of linear accelerator systems is to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0536-2023·2022-12-21
Stradis Healthcare Medical and Surgical Trays Recalled for Incomplete Bag Sealing
Stradis Medical recalls medical and surgical procedure trays and kits due to incomplete outer bag sealing that may compromise sterility. Units were distributed nationwide in the US and Canada.
Product
STRADIS HEALTHCARE, Lipo, Item No.681-254,
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
HighFDA (Devices)·Z-0494-2023·2022-12-21
Surgical Implant Trays Recalled for Incomplete Package Seal
Stradis Healthcare is recalling 162 surgical implant trays distributed nationwide due to incomplete outer bag seals that may compromise sterility.
Product
Surgical room, Implant Pack, Item No.41111UTI, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0499-2023·2022-12-21
Stradis Healthcare Safety Pins Recalled for Potential Sterility Breach
Stradis Healthcare is recalling 1-inch safety pins due to manufacturing defects that may result in incomplete sealing of outer bags, potentially compromising the sterility of medical and surgical procedure kits.
Product
STRADIS HEALTHCARE, SAFETY PINS, SMALL 1" Item No.515-001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0525-2023·2022-12-21
Stradis Healthcare catheter angiography kits recalled for defective sterile sealing
Stradis Medical is recalling catheter angiography procedure kits with potentially incompletely sealed outer bags that may compromise the sterile integrity of the medical devices.
Product
HENRY SCHEIN, CATH ANGIO PACK, Item No.570-2930
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0531-2023·2022-12-21
Medical Surgical Trays and Kits Recalled for Incomplete Outer Bag Sealing
Henry Schein Blue Tail Custom Pack surgical procedure trays are being recalled because manufacturing issues may have caused incomplete sealing of the outer bag, potentially compromising sterility.
Product
HENRY SCHEIN, Blue Tail Custom Pack, Item No.570-3091,
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-0535-2023·2022-12-21
Stradis Healthcare Curved Tip Syringes Recalled Due to Incomplete Sterile Sealing
Stradis Medical is recalling approximately 300 Curved Tip Syringes because manufacturing defects may result in incomplete sealing of the sterile kit, potentially compromising product sterility.
Product
STRADIS HEALTHCARE, CURVED TIP SYRINGE, Item No.60060GCTS,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0468-2023·2022-12-21
Zimmer Recalls NexGen Stemmed Tibial Components Due to Higher Revision Rates
Zimmer Inc. is recalling NexGen Option Stemmed Tibial Components due to clinically and statistically significant higher revision rates when used with specific femoral components. The components are being removed from inventory.
Product
NexGen Option Stemmed Tibial Component Size 5, Item Number 00-5986-047-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0527-2023·2022-12-21
HENRY SCHEIN Amnio Trays Recalled for Incomplete Outer Bag Seal
HENRY SCHEIN Amnio Trays (Item No. 570-3059) manufactured by Stradis Medical are being recalled because the outer bag may be incompletely sealed, potentially compromising the sterility of the medical kit.
Product
HENRY SCHEIN, Amnio Tray, Item No.570-3059,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0551-2023·2022-12-21
Medical Surgical Trays: Incomplete Outer Bag Sealing May Breach Sterility
Stradis Medical is recalling surgical procedure trays due to incomplete sealing of the outer bag, which may compromise the sterility of the kit.
Product
STRADIS HEALTHCARE, Vein, Item No.682-577,
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-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-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-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