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. 1,849 recalls have been distributed to New Mexico in the last 12 months.
Showing 23581–23600 of 48,595 recalls
Recalled Item: Calcium Gluconate 1% Eyewash Oph. Soln Recalled by Pharm D Solutions, LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Gluconate1% Eyewash 10 mg/mL Recalled by Pharm D Solutions, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bi-Mix Injection (Alprostadil 150 mcg/Lidocaine 2 mg/mL) Recalled by Pharm D...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipo MIC-12 Compound Injectable a) NDC 69699-1603-10 Recalled by Pharm D...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenol 7% and Glycerin Aqueous Solution 10 mL Injectable Recalled by Pharm D...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trimix ST-1 30PA-1.5PH-50A Aqueous Solution Pharm D Solutions Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...
The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME)...
The Issue: Firm identified an issue in the manufacturing process which might contribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...
The Issue: Potential for outer pouch sterile barrier to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...
The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Delivers 0.1 mg/day...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.