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. 2,604 recalls have been distributed to Louisiana in the last 12 months.
Showing 17261–17280 of 51,202 recalls
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 1 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 11 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 6 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 5 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Recalled by SCA Pharmaceuticals Due to Subpotency:...
The Issue: Subpotency: Out-of-specification stability test result for low potency was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor)...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good & Gather Banana Chocolate Chip Date & Nut Bars Recalled by Riverside...
The Issue: The product contains an undeclared almonds.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...
The Issue: Device has the potential for fracture during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...
The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Areva Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: based on a Warning Letter received by the manufacturer of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic HVAD Pump Implant Kits Recalled by Heartware, Inc. Due to Pumps...
The Issue: Pumps manufactured with impellers from a subset of lots from a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisafe Distal Duck Kit and Duck Bag Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that certain lots of diluted 4-Zyme may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The cobas z 480 analyzer including dedicated software for IVD Recalled by...
The Issue: Dirty Lens May Cause Invalid or False Positive Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.