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. 2,448 recalls have been distributed to Wyoming in the last 12 months.
Showing 19881–19900 of 27,462 recalls
Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is Recalled by GE...
The Issue: Ferrous material in the SIGNA Pioneer Table Control Box (TCB) could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERION Unit (Vision Planner) Product Usage: The VERION Image Recalled by...
The Issue: Alcon is conducting a voluntary medical device correction of all VERION...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use Recalled by...
The Issue: Endoscope cleaning brush 11276CL may not fit resulting in an inability to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...
The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT-5100 (Epic 5100) and RT 3100 : Product Usage: Recalled by Nidek Inc Due...
The Issue: There has been a reoccurrence of an issue on the RT 5100 and RT 3100 of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...
The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica ISE Module Calibrant A Recalled by AMS Diagnostics, LLC Due to Lot...
The Issue: Lot was not functioning properly and not exhibiting the correct physical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...
The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...
The Issue: The firm has received one report of values for patient height and weight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...
The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...
The Issue: Dialyzer header leak due to possible improper torque
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...
The Issue: After importing, the segmentation results appear mirrored at the CARTO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...
The Issue: PureWick is recalling external catheter for women Wicks because the labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the Recalled by Ab...
The Issue: Wrong quantitative results may be displayed in a report from the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...
The Issue: Out of specification at the thread. The thread height of these screws is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...
The Issue: Out of specification at the thread. The thread height of these screws is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.