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. 2,526 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,526 in last 12 months

Showing 1226112280 of 27,462 recalls

Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Randox Laboratories, Limited

Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...

The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...

The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Zimmer Biomet, Inc.

Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...

The Issue: Potential issue associated with the instrument -end of the shaft could fail...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Enzymatic Creatinine (ECREA) reagent Recalled by Siemens...

The Issue: There is a potential for falsely depressed creatinine results for patients...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 4/0 30 VIO SC-2 124K Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23 Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 3/0 30 VIOLET GS-11 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Enzymatic Creatinine (ECRE_2) reagent Recalled by Siemens...

The Issue: There is a potential for falsely depressed creatinine results for patients...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2-0 UNDYED 30" V-20 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 1 30 VIOLET GS-22 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 12"" VL SS-24 D/A Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing