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. 2,650 recalls have been distributed to Indiana in the last 12 months.
Showing 16581–16600 of 53,528 recalls
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...
The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator....
The Issue: Randox can confirm a positive bias for Total Bilirubin and Direct Bilirubin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...
The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...
The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...
The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sabra Dipping Co Recalled by Sabra Dipping Company, LLC Due to Potential...
The Issue: Potential Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...
The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...
The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...
The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InCore Lapidus Disposable Kit 28mm Left Recalled by Nextremity Solutions Due...
The Issue: Product could potentially contain an undersized inner diameter of the 40mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...
The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InCore Lapidus Disposable Kit 28mm Right Recalled by Nextremity Solutions...
The Issue: Product could potentially contain an undersized inner diameter of the 40mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.