Product Recalls in Illinois

Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,959 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,959 in last 12 months

Showing 21012120 of 30,032 recalls

Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PERI GYN PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: to RES Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to There is a...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) BASIC CATARACT...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PAIN PACK Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) INTUBATION TRAY...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PRECIP TRAY...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) DR. KHAN Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe...

The Issue: During some clinical cases, it has been observed that the SO2 value may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter NovumIQ Syringe INFUSION SYSTEM Recalled by Baxter Healthcare...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY

Recalled Item: Comprehensive Shoulder Stem Recalled by ZIMMER ORTHOPEDICS MANFACTURING...

The Issue: Five complaints received where surgeon was unable to remove and/or connect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Reichert, Inc.

Recalled Item: Phoroptor VRx Digital System Model Numbers: 16241 Recalled by Reichert, Inc....

The Issue: The head of the phoropter head could come loose and potentially detach due...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Reichert, Inc.

Recalled Item: Phoroptor VRx Digital System Model Numbers: 16242 Recalled by Reichert, Inc....

The Issue: The head of the phoropter head could come loose and potentially detach due...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2025· Tandem Diabetes Care, Inc.

Recalled Item: t:slim X2 Insulin Pump with Interoperable Technology Recalled by Tandem...

The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing