Product Recalls in Hawaii
Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,047 recalls have been distributed to Hawaii in the last 12 months.
Showing 15361–15380 of 47,764 recalls
Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 100 units/mL (U-100) Recalled...
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 FlexTouch (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: Fiasp (insulin aspart injection) Recalled by Novo Nordisk Inc Due to...
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: 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: ViCTOZA (liraglutide) injection Recalled by Novo Nordisk Inc Due to...
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: NovoLog FlexPen (insulin aspart) Injection Recalled by Novo Nordisk Inc Due...
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: Saxenda (liraglutide) Injection Recalled by Novo Nordisk Inc Due to...
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: 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: 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: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...
The Issue: Potentially defective component in the AC power adapter which may fail over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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 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: 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.