Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,483 recalls have been distributed to Alabama in the last 12 months.
Showing 21761–21780 of 28,641 recalls
Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...
The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by...
The Issue: The device might fail to detect air in line while infusing the medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...
The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...
The Issue: Reporting feature times out after inactivity for more than an hour sending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...
The Issue: PAL unit has undergone significant technological changes since the previous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...
The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...
The Issue: The firm is conducting a product correction due to an increase in U90-382 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...
The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...
The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...
The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....
The Issue: Airways Development LLC has received a complaint about a canister leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...
The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...
The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: Users can merge a device import file with an image study that already has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...
The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.