Product Recalls in New Mexico
Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,585 recalls have been distributed to New Mexico in the last 12 months.
Showing 4501–4520 of 27,850 recalls
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Structural Balloon Trocar Recalled by Covidien, LP Due...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareEvent Event Management System Recalled by Philips North America Due to...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX (PIC iX) Recalled by Philips North America Due...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.