Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,690 recalls have been distributed to Louisiana in the last 12 months.
Showing 5681–5700 of 29,201 recalls
Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...
The Issue: Device is breaking while in use, potential for patients to require a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...
The Issue: There is the potential that the safety shield may not properly engage on IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...
The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...
The Issue: Various medical devices potentially exposed to rodent and rodent activity....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinchlock SS Knotless Anchor Inserter Recalled by Stryker Corporation Due to...
The Issue: Expired Product distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Knee insert...
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: 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: 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.