Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,685 recalls have been distributed to Missouri in the last 12 months.
Showing 5701–5720 of 29,298 recalls
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: 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.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...
The Issue: XXX
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 PBDS Recalled by Cardinal Health 200, LLC Due...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.