Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,543 recalls have been distributed to Nebraska in the last 12 months.
Showing 15941–15960 of 28,140 recalls
Recalled Item: BOX VWR ZESTAW DO VATS KLIN Product Usage: The Endo Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm - Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" 45mm Gray Curved Tip Articulating Vascular Reload with Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KIT1171C KIT LAP CYSTECTOMY Product Usage: The Endo GIA Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX PST03533 KIT APP STAPLER Product Usage: The Endo GIA Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX PST03699 KIT APP MED ALTERNATIV STAP Product Usage: The Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX LAPZD ZESTAW DO SG (2) BOX LAPISG1 ZESTAW Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX HEMIGX1 ZESTAW DO HEMICOLECTOMII (Item Number HEMIGX1 ZESTAW DO...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX TGGLOGOWX1 DO TOTAL GASTRECTOMIII Product Usage: The Endo GIA Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec Esteem(TM) Synergy Stomahesive(R) Recalled by ConvaTec, Inc Due to...
The Issue: It was discovered that the stoma hole of one lots of the Esteem synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.