Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,396 recalls have been distributed to South Dakota in the last 12 months.
Showing 20101–20120 of 27,558 recalls
Recalled Item: (Stryker) AccuPlace Round Level Needle Guide Recalled by Stryker Instruments...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...
The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...
The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...
The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...
The Issue: Potential data loss occurs as a result of the software archiving not working...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge FlexConnect software Recalled by Merge Healthcare, Inc. Due to...
The Issue: Communication protocols interfacing with the affected software version with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...
The Issue: A migrated study that has annotations will display the annotations, but when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...
The Issue: The software was not presenting the PURE filter user interface message on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access used with Merge PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is an integrated Recalled...
The Issue: Patient information in the header is only found on the first page of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Product was distributed under the AMICAS label Recalled...
The Issue: The patient name in the Halo title bar and the thumbnails do not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PINPOINT Endoscopic Fluorescence Imaging System Recalled by Novadaq...
The Issue: It has been determined that the PINPOINT Operator's Manual does not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video...
The Issue: The firm has become aware of the potential for disruption (flickering) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crosslock DVR ePAK -Sterile Recalled by Biomet, Inc. Due to Foreign Object...
The Issue: Components of the DVR ePAKs can oxidize during shipment and storage prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular System Product Usage - Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: software for Syngo Dynamics a Picture Archiving and Communication System...
The Issue: Siemens is releasing a software update that addresses an issue of mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular Shell Product Usage: Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orapharma (Onpharma) Onset Mixing Pen Rx only Recalled by Valeant...
The Issue: It has been determined that the Onset Mixing Pen has an optimal use period...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.