Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 26581–26600 of 51,038 recalls
Recalled Item: ADVANSYS TTC Recalled by NewDeal SA Due to Use of the impacted product may...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple...
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: ADVANSYS MLP/DLP Recalled by NewDeal SA Due to Use of the impacted product...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia 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: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...
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: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...
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 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology...
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 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...
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: Large QWIX Recalled by NewDeal SA Due to Use of the impacted product may...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology...
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 Articulating Vascular Reload with Tri-Staple Technology...
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: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIBIAXYS Recalled by NewDeal SA Due to Use of the impacted product may cause...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling...
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 45 mm Extra Thick Black Articulating Reload with Tri-Staple...
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: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...
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.