Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,609 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,609 in last 12 months

Showing 1344113460 of 28,488 recalls

Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 Reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

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

Class II — Potential Health HazardOngoing
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