Illinois recalls
4003 federal recalls on file affecting Illinois - 927 Illinois-specific plus 3076 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-14FDA-DevicePhilipsClass IINationwideCheck your Philips MX40 patient monitor
It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.
- 2026-01-14FDA-DeviceSecuritas HealthcareClass IINationwideCheck your Securitas Healthcare call station
Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.
- 2026-01-14FDA-DeviceSecuritas HealthcareClass IINationwideCheck your Securitas Arial call station battery alerts
Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.
- 2026-01-14FDA-DeviceAbiomedClass IINationwideCheck Abiomed Impella 5.5 packaging
Device packaged in incorrect outer box carton.
- 2026-01-14FDA-DeviceSophysaClass IINationwideStop using Sophysa Pressio 2 ICP monitors
Customer complaints of Pressio monitor rebooting.
- 2026-01-14FDA-DeviceCareFusionClass IINationwideCheck your BD Pyxis ES Enterprise Server
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
- 2026-01-14FDA-DeviceRemote Diagnostic TechnologiesClass IINationwidePhilips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual
Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If healthcare providers base clinical judgment on unvalidated measurements, this could potentially lead to incorrect clinical decisions.
- 2026-01-14FDA-DeviceBeckman CoulterClass IINationwideContact Beckman Coulter about UniCel Dxl 800 analyzer
Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.
- 2026-01-14FDA-DeviceBeckman CoulterClass IINationwideContact Beckman Coulter about your UniCel DxL 600
Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.
- 2026-01-14FDA-DeviceMeridian BioscienceClass IINationwideStop using Meridian Revogene C. difficile test
The affected lots show a decline in performance over time, which may lead to false-negative results.
- 2026-01-14FDA-DeviceRoche DiagnosticsClass IINationwideContact your lab if you used Roche Elecsys Anti-TSHR
Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment.
- 2026-01-14FDA-DevicePhilipsClass IINationwideStop using affected Philips Incisive CT scanners
Potential for incomplete scan due to unstable connection inside of floating sensor.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideDo not use Halyard MINI PLUS KIT SOUTH
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideDo not use Halyard ORGAN RECOVERY OR PACK
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideStop using Halyard ORGAN RECOVERY OR PACK
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS X-ray system
A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.
- 2026-01-14FDA-DeviceVision RTClass IINationwideCheck AlignRT InBore documentation for laser details
Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted from the Instructions for Use for the subject system as required by 21 CFR 1040,10(h), via conformance with recognized consensus standard IEC 60825-1 Ed. 3 (FDA Laser Notice 56).
- 2026-01-14FDA-FoodMeijerClass IIStop using Meijer Steam Distilled Water
Floating black foreign substance in the product
- 2026-01-14FDA-FoodMAYEJClass IINationwideStop using MAYEJ Italian Parsley
pathogen Cyclospora cayetanensis
- 2026-01-14FDA-FoodDirect Source SeafoodClass IIDon't eat Market 32 frozen raw shrimp
Shrimp may be contaminated with Cesium-137 (Cs-137).
- 2026-01-14FDA-FoodDirect Source SeafoodClass IIwaterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Product is packaged in white flexible plastic pouch with multicolored labeling. UPC is 0 21130 13224 9. Product of Indonesia. DISTRIBUTED BY LUCERNE FOODS, INC. P.O. BOX 99 PLEASANTON, CA 94566.
Shrimp may be contaminated with Cesium-137 (Cs-137).
- 2026-01-14FDA-FoodZiyadClass IINationwideStop eating Baraka Gourmet Pastry Kunafe
May contain partially hydrogenated oils
- 2026-01-14FDA-FoodZiyadClass IINationwideCheck your Baraka puff pastry for recall
May contain partially hydrogenated oils
- 2026-01-14FDA-FoodMcCainClass IIStop using Sysco Imperial Potato Tater Barrel
Clear hard plastic fragments.
- 2026-01-14FDA-FoodMcCainClass IIStop using Ore-Ida Tater Tots item OIF00215A
Clear hard plastic fragments.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Ambriola Piccante Pecorino Romano cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano Grated cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Sam's Pecorino Romano grated cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano cheese
Product tested positive for Listeria Monocytogenes.
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