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. 1,077 recalls have been distributed to Indiana in the last 12 months.
Showing 16721–16740 of 53,528 recalls
Recalled Item: Levemir FlexTouch (insulin detemir) injection Recalled by Novo Nordisk Inc...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xultophy 100/3.6 (insulin degludec and liraglutide injection) Recalled by...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fiasp PenFill (insulin aspart injection) 100 units/mL (U-100) Recalled by...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Macleods Pharma Usa Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectrum Medical Quantum Standard heat exchanger Recalled by QURA S.R.L. Due...
The Issue: Product labeled as sterile may not have been adequately sterilized. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Land O Lakes Queso Bravo White Cheese Dip with Jalapeno Recalled by Land...
The Issue: Queso Cheese dip may contain foreign material (metal).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bobo's Maple Pecan Oat Bars Recalled by Simply Delicious Inc. Due to Two...
The Issue: Two consumer complaints were received for peanuts in maple pecan bars.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- Recalled by...
The Issue: One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...
The Issue: Users may observe additional locus specific signals at 9q34. The device pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...
The Issue: Siemens has become aware of a potential issue with software version VE20C....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.