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. 2,932 recalls have been distributed to Illinois in the last 12 months.
Showing 5901–5920 of 30,032 recalls
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apellis Injection Kit 29g Injection Needle -single use intended to Recalled...
The Issue: 19-gauge x 1" inch filter needles showed appearances of a small fraction of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett Cuff Pressure Manager Recalled by Covidien Due to Inadequate...
The Issue: Inadequate internal fixation of the power inlet port to the cuff pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used Recalled...
The Issue: Handbook Revision (Rev13) a dilution step is indicated as an Action when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm...
The Issue: Some catheter kits labeled as 23 cm implant length incorrectly included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid Readout Biological Indicator Recalled by 3M Company -...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid Readout Steam Challenge Pack Recalled by 3M Company -...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPMI LUMERA 300 Recalled by Carl Zeiss Suzhou Co., Ltd. Due to Surgical...
The Issue: Surgical microscope for use in ophthalmology may be missing a screw from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Constellation Vision System Recalled by Alcon Research, LLC Due to...
The Issue: Ophthalmic microsurgical vision systems have a new Printed Circuit Board...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOZO Bilateral Arm L-Dex Software Recalled by Impedimed Limited Due to...
The Issue: Bilateral L-Dex assessment software does not have the same level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: exoplan version 3.1 Rijeka Software -A medical software Recalled by Exocad...
The Issue: A software library filtering error has been discovered which occurs when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX with Software Version Number 4.x in Recalled...
The Issue: Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.