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. 1,026 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,026 in last 12 months

Showing 16181–16200 of 48,595 recalls

Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 25G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: SD-240U-10 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 3MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: CRESCENT SNARE Recalled by Aomori Olympus Co., Ltd. Due to Inspection...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX LOWER 25G 2.5MM Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: B-V443Q-A 3-LUMEN EXTRACTION BALLOON V Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX LOWER 23G 4MM Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-601D-1519 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 5MM Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET Recalled by Aomori Olympus Co.,...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-411D-1321 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 23G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: SD-210U-25 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2021· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2021· Ittella International, LLC

Recalled Item: Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life...

The Issue: A gluten free claim was inadvertently used on the lid of the container....

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 1, 2021· Precision Dose Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse USP 0.12% Recalled by Precision Dose Inc....

The Issue: cGMP deviations: The firm was notified of the manufacturer's expanded recall.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· Allergan, PLC.

Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...

The Issue: Labeling: Missing instructions for use insert

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· AuroMedics Pharma LLC

Recalled Item: Acetaminophen Injection 1 Recalled by AuroMedics Pharma LLC Due to...

The Issue: Discoloration and failed pH specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 30, 2020· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...

The Issue: The Quality Control (QC) card has a label error for the standard deviation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2020· Baxter Healthcare Corporation

Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...

The Issue: Potential for the battery to lose its ability to be recharged.

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

Class II — Potential Health HazardOngoing