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. 1,866 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,866 in last 12 months

Showing 2102121040 of 48,595 recalls

DrugJune 24, 2019· H J Harkins Company Inc dba Pharma Pac

Recalled Item: Diphenhydramine HCL Liquid Recalled by H J Harkins Company Inc dba Pharma...

The Issue: Microbial Contamination of Non-sterile Products: Potential product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2019· Fenwal Inc

Recalled Item: Vigilant Agilia Recalled by Fenwal Inc Due to The firm is correcting four...

The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2019· Fenwal Inc

Recalled Item: VOLUMAT MC AGILIA US Recalled by Fenwal Inc Due to The firm is correcting...

The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Model # 728231 Recalled by Philips Medical Systems (Cleveland)...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model # 728323 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to In certain...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to In...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT Model # 882456 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT SP Model # 728311 Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Model # 728321 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Vereos PET/CT Model # 882446 Recalled by Philips Medical Systems (Cleveland)...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT Model # 728332 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Cardiocommand Inc.

Recalled Item: TAPSYSTEM Model 2A Recalled by Cardiocommand Inc. Due to There is a...

The Issue: There is a potential for an assembly error resulting in the battery wire...

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

Class III — Low RiskOngoing
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: GENCONTUSS (Chlorpheniramine Maleate Recalled by Pharma-Natural Inc. Due to...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Dayma SUPER FORTE XL10 (Camphor 0.5% Recalled by Pharma-Natural Inc. Due to...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg Recalled by Pharma-Natural Inc....

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%) Recalled by...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%) Recalled by...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% &...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: SORBUGEN NR (Dextromethorphan HBr Recalled by Pharma-Natural Inc. Due to...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund