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. 1,872 recalls have been distributed to New Mexico in the last 12 months.
Showing 20441–20460 of 27,850 recalls
Recalled Item: 2.3mm Turbo-Power OTW Recalled by Spectranetics Corp. Due to The product is...
The Issue: The product is labeled with an expiration date that is past its shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jadak Barcode Scanner Recalled by CareFusion 303, Inc. Due to Customers...
The Issue: Customers reported issues when scanning medications with the scanners. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Battery Charger II (UBC II) Recalled by The Anspach Effort, Inc....
The Issue: The device is reported to enter safe mode and is no longer able to charge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for...
The Issue: Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...
The Issue: OraSure Technologies, Inc. discovered the package insert included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS Automated Blood Coagulation Analyzer System Recalled by Siemens...
The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS XP Automated Blood Coagulation Analyzer System Recalled by Siemens...
The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000¿ is...
The Issue: When a user performed radiography using the wireless FPD, a message window...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Estradiol Test Code E2 Catalog Number: LKE21 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Estradiol Test Code E2 Catalog Number: K6463 Recalled...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 EstradiolTest Code E2 Catalog Number: L2KE22 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number:...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF...
The Issue: The Firm has discovered a Software bug.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super Arrow-Flex Percutaneous Sheath Introducer Sets or CL-07635 Recalled by...
The Issue: Arrow has issued a recall for these products due to potential packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 60 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 63 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 70 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 66 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 20 consists of all prod oct under poduct code: Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-FLEX Option FEM NexGen CR-FLEX Precoat FEM NexGen CR-FLEX Recalled...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.