Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,012 recalls have been distributed to Indiana in the last 12 months.
Showing 36441–36460 of 53,528 recalls
Recalled Item: Vaxcel PICC with PASV Introducer Kit under the following labels: 1) 4F...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV Intermediate Safety MST Kit under the Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela PICC with PASV Valve Technology Catheter Kit Recalled by Navilyst...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV MST-60 Kit under the following labels: 1) 3F Recalled...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV MST-30 Kit under the following labels: 1) 4F Recalled...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is Recalled by Ossur H /...
The Issue: There is a potential for partial or complete fracture of the plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...
The Issue: Integra's post QA release review of historical product release test results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...
The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After importing segmentation results of the left atrium created on the Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...
The Issue: The units have been fitted with a potentially faulty power supply cable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SODIUM IODIDE I 131 CAPSULE Recalled by Jubilant Draximage Inc Due to...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient Recalled...
The Issue: CGMP Deviations: active pharmaceutical ingredient intermediates failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.