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. 2,776 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,776 in last 12 months

Showing 2114121160 of 55,304 recalls

FoodJanuary 7, 2020· Golden State Foods

Recalled Item: Taco Bell Creamy Jalapeno Sauce Recalled by Golden State Foods Due to...

The Issue: Notification by supplier of a recall of starch ingredient due to metal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2020· Golden State Foods

Recalled Item: Pizza Hut Garlic Dipping Sauce Recalled by Golden State Foods Due to...

The Issue: Notification by supplier of a recall of starch ingredient due to metal...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2020· Ingredion Incorporated

Recalled Item: Ingredion ULTRA-TEX4 Food Starch in 50lb paper bags Recalled by Ingredion...

The Issue: Foreign material. Potential for fragments of stainless steel wire in the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Ethicon, Inc.

Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...

The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Zimmer Surgical Inc

Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...

The Issue: When inflating/deflating a single bladder, both bladders could potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· Clinical Diagnostic Solutions, Inc.

Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...

The Issue: A mix-up of autosampler tube positions with a possibility of...

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

Class II — Potential Health HazardOngoing
FoodJanuary 2, 2020· purely elizabeth.

Recalled Item: purely elizabeth Chocolate Sea Salt probiotic granola. Net Wt. 8 Recalled by...

The Issue: Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing