Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,562 recalls have been distributed to Nevada in the last 12 months.
Showing 18201–18220 of 28,334 recalls
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N230) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN70) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P634) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N340) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P605) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Streptococcus Susceptibility card (AST-ST01) Recalled by...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P648) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N325) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N353) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Fungal Susceptibility card (AST-YS08) Recalled by Biomerieux Inc...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN67) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N330) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Frequency Resection Electrodes Recalled by Olympus Corporation of the...
The Issue: Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue OR Towels Recalled by Medical Action Industries Inc Due to Lint present...
The Issue: Lint present on sterile Operating Room Towels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White OR Towels Recalled by Medical Action Industries Inc Due to Lint...
The Issue: Lint present on sterile Operating Room Towels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...
The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...
The Issue: nail not properly engaging with the targeting jig due to certain undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.