State

Illinois product recalls

72,933 recalls have nationwide distribution and so reach Illinois. 11,603 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,603
Critical: 2,039
Severe: 2,516
Most recent: 2026-09-09

Of the 11,603 recalls naming Illinois we have scored against our rubric, 2,039 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,516 (22%) are Severe.

Which agencies issued them

These figures cover only the 11,603 recalls whose distribution notice names Illinois specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2776–2800 of 84536

HighFDA (Devices)·Z-1640-2026·2026-04-01
Olympus PK cutting forceps jaws may break from defective welds
Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation dur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0406-2026·2026-04-01
Teva octreotide acetate injection recalled over sterility assurance deficiencies
Teva is recalling twelve lots of Octreotide Acetate for Injectable Suspension after quality system deficiencies were identified during an FDA inspection at the contract manufacturer.
Product
OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1638-2026·2026-04-01
Olympus Everest bipolar forceps model 3005 jaws may break
Olympus is recalling Everest Bipolar Cutting Forceps model 3005 because a supplier did not adequately validate the welding process, and defective welds can cause the jaw to break during clinical use.
Product
Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3005 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved u
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2026·2026-04-01
I.T.S. volar radius plates heat more in MRI than stated
I.T.S. GmbH is recalling Volar Radius Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2026·2026-04-01
GE Imactis CT navigation may show needle trajectory that differs from actual
GE Medical Systems is recalling the Imactis CT-Navigation System because of a potential discordance between the simulated needle trajectory and tip position and the actual trajectory and tip position.
Product
Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1630-2026·2026-04-01
Orthalign knee drill plates may allow a bone cut exceeding specification
Orthalign is recalling one lot of the Trimax Pegged Drill Plate for the Lantern Knee System because plates manufactured out of specification can result in a bone cut in excess of 0.0800 inches.
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1632-2026·2026-04-01
Straumann custom abutments made from wrong bar material after mix-up
Straumann is recalling Custom Abutment Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.
Product
Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1613-2026·2026-04-01
Olympus OER-Pro reprocessor no longer compatible with two valve models
Olympus is recalling the OER-Pro Endoscope Reprocessor because the MAJ-1443 and MAJ-1444 air/water valves are no longer reprocessing compatible with the OER-Pro and OER-Elite reprocessors.
Product
Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0615-2026·2026-04-01
Savannah Bee Company Honey BBQ Sauce Mustard Undeclared Allergens
Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.
Product
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED VINEGAR, WATER, MUSTARD SEED, SALT, SPICES (INCLUDING PAPRIKA AND TUMERIC), NATURAL FLAVOR, GARLIC), HONEY, WATER, DISTILLED VINEGAR, SUGAR, TOMATO CONCENTRATE, HA
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-1595-2026·2026-04-01
I.T.S. calcaneus repair plate heats more in MRI than stated
I.T.S. GmbH is recalling the FR.O.H. Calcaneus Repair System anterolateral calcaneus plate because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1602-2026·2026-04-01
I.T.S. distal humeral plates heat more in MRI than stated
I.T.S. GmbH is recalling Distal Humeral Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers. 1. Cortical Screw, Locking; Article Numbers: 37351-10-N, 37351-12-N, 37351-14-N, 37351-16-N, 37351-18-N, 37351-20-N, 37351-22-N, 37351-24-N, 37351-26-N, 37351-28-N, 373
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1633-2026·2026-04-01
Straumann angled custom abutments made from wrong bar material
Straumann is recalling Custom Abutment AS Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.
Product
Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1605-2026·2026-04-01
I.T.S. foot locking plates heat more in MRI than stated
I.T.S. GmbH is recalling the FLS Foot Locking Plates System and HOL Hallux Osteotomy Locking Plate because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with the below descriptions and corresponding article numbers. 1. FLS - Foot Locking Plates System, Cancellous Stabilization Screw; Article Numbers: 37303-10, 37303-12, 37303-14, 37303-16, 37303-18, 373
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1644-2026·2026-04-01
Olympus PKS cutting forceps jaws may break from defective welds
Olympus is recalling PKS Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visuali
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1598-2026·2026-04-01
I.T.S. straight and forearm plates heat more in MRI than stated
I.T.S. GmbH is recalling Straight Plates with Angular Stability, including forearm and compression plates, because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article numbers. 1. Forearm Plate, Curved; Article Numbers: 21604-6, 21604-9. 2. Forearm Plate, Straight; Article Numbers: 21605-11, 21605-6, 21605-9. 3. Straight Compression Pla
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1596-2026·2026-04-01
I.T.S. pilon and tibia plates heat more in MRI than stated
I.T.S. GmbH is recalling Pilon Plates with Angular Stability and Anterolateral Tibia Plates because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral Tibia Plate; Article Numbers: 21311-11, 21311-15, 21311-7, 21312-11, 21312-15, 21312-7. 2. Pilon Plate 4mm; Article Numbers: 21094-10, 21094-4, 21094-6, 2109
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1634-2026·2026-04-01
TECNIS Eyhance intraocular lens haptic may stick to the optic
AMO Puerto Rico Manufacturing is recalling TECNIS Eyhance IOLs with the TECNIS Simplicity Delivery System because a limited quantity may have a haptic that sticks to the optic, preventing consistent unfolding.
Product
Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Model/Catalog Number: DIB00 Software Version: N/A Product Description: The TECNIS SIMPLICITY" Delivery System is designed to provide
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1603-2026·2026-04-01
I.T.S. femur and tibia plates heat more in MRI than stated
I.T.S. GmbH is recalling the LRS Locking Reconstruction System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corresponding article numbers. 1. DFL (Distal Femur Locking) Distal Femur Plate; Article Numbers: 21301-5, 21301-7, 21301-9, 21301-13, 21302-5, 21302-7, 21302-9, 21302-13. 2. PTL (Proximal Lateral
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0589-2026·2026-04-01
Chilli Spanish Peanuts First Street recalled for glass contamination
Western Mixers Produce & Nuts, Inc. is recalling First Street Chilli Spanish Peanuts (11 oz) because glass fragments were found in sealed containers. Affected lots have expiration dates of 2/11/2027, 2/13/2027, and 2/23/2027.
Product
Chilli Spanish Peanuts, First Street brand, 11oz clear plastic container. UPC: None Item Code: 2608-T20
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1599-2026·2026-04-01
I.T.S. cannulated screw system heats more in MRI than stated
I.T.S. GmbH is recalling the I.T.S. Screw System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
I.T.S. Screw System with the below descriptions and corresponding article numbers. 1. Cancellous Screw, Cannulated; Article Numbers: 31404-16, 31404-18, 31404-20, 31404-22, 31404-24, 31404-26, 31404-28, 31404-30, 31404-32, 31404-34, 31404-36, 31404-38, 31404-40, 31404-42, 314
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1608-2026·2026-04-01
I.T.S. pelvic reconstruction plates heat more in MRI than stated
I.T.S. GmbH is recalling the Pelvic Reconstruction System PRS RX and PRS Phoenix because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
Brand Name: I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix) with the below descriptions and corresponding article numbers. 1. Anterior Column Plate; Article Numbers: 21218-16, 21219-16. 2. Anterior Column Plate; Article Numbers: 21218-14, 21219-14. 3. Biplanar 2-C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1594-2026·2026-04-01
I.T.S. proximal humeral plates heat more in MRI than stated
I.T.S. GmbH is recalling the Humeral Head Plate with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Brand Name: Humeral Head Plate with Angular Stability, with the following description: Proximal Humeral Plate. Article Numbers: 211341-10, 211341-4, 211341-7, 21134-4, 21134-5, 21135-4, 21136-4, 21136-5, 21136-7, 21137-4, 21137-7, 21138-4, 21139-4.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V209000·2026-04-01
Audi Q3 recalled over remote sunroof closing from out of sight
Volkswagen Group of America is recalling 6,077 Audi Q3 vehicles because incorrect software may allow remote sunroof closing from a distance where the operator cannot clearly see the sunroof.
Product
AUDI — AUDI Q3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1611-2026·2026-04-01
Olympus endoscope air water valves no longer compatible with named reprocessors
Olympus is recalling the MAJ-1444 Endoscope Air/Water Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Product
Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V207000·2026-04-01
Mack Recalls 2025-2027 Trailers Due to Turn Signal Software Defect
Mack Trucks is recalling 2025-2027 Pioneer and 2027 Anthem trailers because turn signals may not function properly, increasing crash risk.
Product
MACK — MACK PIONEER PR (4), ANTHEM AN (4)
Category
Vehicle
Distribution
Distributed nationwide