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. 2,579 recalls have been distributed to New Mexico in the last 12 months.
Showing 5301–5320 of 27,850 recalls
Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...
The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...
The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit- For access to the subarachnoid space Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...
The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...
The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...
The Issue: Due to an increased risk of degradation of the power entry switch resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS icono (ceiling configuration) Recalled by Siemens Medical Solutions...
The Issue: Potential hardware issue for ARTIS icono ceiling system: collision sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: Routine quality control testing of affected blood culture identification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...
The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novum IQ Syringe infusion system Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits:...
The Issue: Produced with unintended open slits on the side of the mouthpiece body, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190 Recalled by Olympus...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number Q180-AC...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.