Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,357 recalls have been distributed to Wyoming in the last 12 months.
Showing 33341–33360 of 48,219 recalls
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: 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 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: 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 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: 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: 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: 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: 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.
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: 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: 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: Raw Meal Organic Vanilla Powder Recalled by Garden Of Life Llc Due to...
The Issue: Products possibly contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Meal Organic Original Powder Recalled by Garden Of Life Llc Due to...
The Issue: Products possibly contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Meal Organic Chocolate Powder Recalled by Garden Of Life Llc Due to...
The Issue: Products possibly contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Meal Organic Vanilla Spiced Chai Powder Recalled by Garden Of Life Llc...
The Issue: Products possibly contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Apple Caramel Almond Tea Recalled by International Tea Importers Due to...
The Issue: International Tea Importers is recalling Apple, Caramel & Almond Tea because...
Recommended Action: Do not consume. Return to store for a refund or discard.