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. 2,694 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,694 in last 12 months

Showing 4008140100 of 55,304 recalls

Medical DeviceSeptember 28, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...

The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....

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

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2015· Tf Supplements

Recalled Item: RHINO 7 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Tf Supplements

Recalled Item: Rhino 7 Platinum 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Actavis...

The Issue: Failed Dissolution Specifications: Low Out-of-Specification results for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2015· Stryker Spine

Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...

The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...

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

Class II — Potential Health HazardOngoing
DrugSeptember 24, 2015· Pfizer Inc.

Recalled Item: Xanax (alprazolam) tablets Recalled by Pfizer Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2015· Airways Development LLC

Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....

The Issue: Airways Development LLC has received a complaint about a canister leaking...

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

Class II — Potential Health HazardOngoing
DrugSeptember 23, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Shorts on The Beach Strong Formula by Pink Bikini capsules Recalled by...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 23, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Pink Bikini Strong Formula capsules Recalled by Lucy's Weight Loss (dba....

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 23, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Shorts on The Beach Golden Edition by Pink Bikini Recalled by Lucy's Weight...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 23, 2015· CSM Bakery Products NA

Recalled Item: Daily Chef Peanut Butter Bars Recalled by CSM Bakery Products NA Due to...

The Issue: Foreign matter (rigid plastic pieces) found in peanut butter bars.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2015· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...

The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· GE Medical Systems, LLC

Recalled Item: MR Surgical Suite II Table Recalled by GE Medical Systems, LLC Due to GE...

The Issue: GE became aware of an issue with the table transfer release mechanism of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· Berchtold Corp.

Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...

The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 22, 2015· Midway Importing, Inc

Recalled Item: Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets...

The Issue: Cross Contamination With Other Products: Potential cross-contamination of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software with Issuer of Patient ID (IPID). The Recalled by...

The Issue: For sites using the Issuer of Patient ID (IPID), the system will display the...

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

Class II — Potential Health HazardOngoing