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. 2,590 recalls have been distributed to Oregon in the last 12 months.
Showing 14441–14460 of 28,488 recalls
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Sponge with the following product description and model numbers:...
The Issue: Potential lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Syringe Administration Set-Product Package Size 50 Recalled by...
The Issue: Leaking of the Smartsite Syringe Administration Set. May result in delay or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Small Diameter Cement Plug Inserter-Sterile Recalled by Zimmer...
The Issue: Lack of an adequate sterilization validation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnidiagnost Classic Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva w/ Flat Detector Recalled by Philips North America, LLC...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URODiagnost Eleva Recalled by Philips North America, LLC Due to The locking...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urodiagnost Recalled by Philips North America, LLC Due to The locking plate...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine & Trauma 3D Navigation 1.0 (subpart of the system Recalled by Brainlab...
The Issue: In certain occurrences, the affected navigation software application might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity c Processing Module LN 03R67-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.