Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,544 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,544 in last 12 months

Showing 1336113380 of 27,833 recalls

Medical DeviceJuly 1, 2019· Privapath Diagnostics Ltd

Recalled Item: Universal Sexual Health Testing Kit Recalled by Privapath Diagnostics Ltd...

The Issue: A supplier informed PrivaPath Diagnostics that there is a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2245 - Product Usage: Kit is Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: LACERATION TRAY Kit Code: SUT18370 - Product Usage: Kit is Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: SNAG FREE SUTURE TRAY Kit Code: SUT14355 - Product Usage: Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: UNIVERSAL BLOCK TRAY Kit Code: MNS6645 - Product Usage: Kit Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: DRIVELINE MANAGEMENT TRAY Kit Code: DT17780B - Product Usage: Kit Recalled...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: NEONATAL PICC INSERTION TRAY Kit Code: CVI2310 - Product Usage: Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: LVAD DRESSING SYSTEM W/BIOPATCHKit Code: DM700 - Product Usage: Kit Recalled...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: HIGH DRAINAGE LVAD TRAY Kit Code: DM950 - Product Usage: Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2650H - Product Usage: Kit is Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: STERILE FLUORO SSP TRAY Kit Code: MNS11605 - Product Usage: Recalled by...

The Issue: Potential for sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Teleflex Medical

Recalled Item: Rusch EasyCath Kit Recalled by Teleflex Medical Due to Potential for product...

The Issue: Potential for product not to be sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Clariance Inc

Recalled Item: Erisma- LP posterior fixation system with the below specifically affected...

The Issue: Potential for the polyaxial screw to become disassembled during implant.

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

Class III — Low RiskOngoing
Medical DeviceJune 28, 2019· Sentinel CH SpA

Recalled Item: MULTIGENT Lithium-intended for the quantitation of lithium in serum or...

The Issue: Added an additional SmartWash parameter for the Lithium and Alinity c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Sentinel CH SpA

Recalled Item: Alinity c Lithium Reagent Kit- intended for the quantitation of Recalled by...

The Issue: Added an additional SmartWash parameter for the Lithium and Alinity c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing