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. 1,078 recalls have been distributed to New Mexico in the last 12 months.
Showing 10401–10420 of 27,850 recalls
Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix" PMIC-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software...
The Issue: When using software 1.90.2.09 or 1.90.8.06 and using modality worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** spineX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...
The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Medela .0193 AXS Universal Aspiration Tubing (01)07612367053921 -...
The Issue: Incorrect expiration date of "2023-07-24" on label of sterile tubing....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 3"x100'. One roll per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Prof (Professional) Meters- IVD professional healthcare...
The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.