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. 2,567 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,567 in last 12 months

Showing 76417660 of 48,595 recalls

Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number:...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Small intestinal videoscope-For endoscopy and endoscopic surgery within the...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Colonoscope: for endoscopy and endoscopic surgery within the lower digestive...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Ultrasonic gastrovideoscope-Real time ultrasound imaging Recalled by Aizu...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Mobile airway scope-diagnosis and observation to access airway anatomy...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Hysteroscope-For endoscopic diagnosis within the uterus Model Number:...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the...

The Issue: Channel air drying process was not validated, and that a small percentage of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Securitas Healthcare LLC

Recalled Item: Arial Water Resistant Pendant with Long Wristband Recalled by Securitas...

The Issue: Premature battery depletion presents a risk that alarms will not be received...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Securitas Healthcare LLC

Recalled Item: Arial Water Resistant Pendant with Wristband Recalled by Securitas...

The Issue: Premature battery depletion presents a risk that alarms will not be received...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Securitas Healthcare LLC

Recalled Item: Arial Water Resistant Pendant with Neck Lanyard Recalled by Securitas...

The Issue: Premature battery depletion presents a risk that alarms will not be received...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2023· Townsend Design

Recalled Item: SPRYSTEP VECTOR KAFO Recalled by Townsend Design Due to Due to potential air...

The Issue: Due to potential air pockets between layers of material, their is the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2023· Townsend Design

Recalled Item: CUSTOM SPRYSTEP Recalled by Townsend Design Due to Due to potential air...

The Issue: Due to potential air pockets between layers of material, their is the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2023· Townsend Design

Recalled Item: SPRYSTEP VECTOR Recalled by Townsend Design Due to Due to potential air...

The Issue: Due to potential air pockets between layers of material, their is the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2023· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...

The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...

The Issue: There have been reports of patients suffering arrhythmias, reported as short...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: HYDROmorphone in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL 2 mcg/mL and bupivacaine 0.125% PF in 0.9% sodium Recalled by...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund