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. 1,046 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,046 in last 12 months

Showing 14981–15000 of 48,595 recalls

Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
DrugMay 21, 2021· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide oil) 0.01% Ear Drops 20 mL bottles...

The Issue: Presence of Foreign Substance: Potential for broken glass within the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: The number of customer complaints for ripping...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: The number of customer complaints for ripping...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 20, 2021· The Binding Site Group, Ltd.

Recalled Item: FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems Recalled...

The Issue: The high and low level "Quality Controls" demonstrate a positive bias of...

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

Class II — Potential Health HazardOngoing
FoodMay 20, 2021· Interstate Food Products, LLC

Recalled Item: Little Hatch's Roasted Chili Salsa - Hot Recalled by Interstate Food...

The Issue: Product samples tested positive for Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2021· Interstate Food Products, LLC

Recalled Item: Little Hatch's Jalapeno Cream Cheese Recalled by Interstate Food Products,...

The Issue: Product samples tested positive for Listeria monocytogenes. The products...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2021· Interstate Food Products, LLC

Recalled Item: Little Hatch's Spicy Queso Recalled by Interstate Food Products, LLC Due to...

The Issue: Product samples tested positive for Listeria monocytogenes. The products...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2021· Interstate Food Products, LLC

Recalled Item: Little Hatch's Queso Recalled by Interstate Food Products, LLC Due to...

The Issue: Product samples tested positive for Listeria monocytogenes. The products...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 19, 2021· Philips Medical Systems DMC GmbH

Recalled Item: ProxiDiagnost N90. radiography and fluoroscopy system Recalled by Philips...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Bard Access Systems Inc.

Recalled Item: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard...

The Issue: Catheter convenience kits contain the incorrect guidewire. Kits were labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Vero Biotech, LLC

Recalled Item: GENOSYL DS Recalled by Vero Biotech, LLC Due to Reports received of NO...

The Issue: Reports received of NO measured below desired dose during transition between...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Arrow International Inc

Recalled Item: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm Recalled...

The Issue: Marketed without a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Recalled by...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Arrow International Inc

Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr....

The Issue: Marketed without a 510K

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

Class II — Potential Health HazardOngoing