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. 2,457 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,457 in last 12 months

Showing 2742127440 of 50,914 recalls

Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray)...

The Issue: Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2018· ALLERGAN

Recalled Item: NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets Recalled by...

The Issue: Labeling: Not Elsewhere Classified: does not have the required "CII"...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Metformin Hydrochloride Tablets Recalled by Aurobindo Pharma Ltd. Due to...

The Issue: Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodFebruary 2, 2018· Ross Acquisitions Company

Recalled Item: STAR WARS TIN WITH CARAMEL POPCORN NET WT 3.5 oz (99g) CONTAINS MILK AND SOY...

The Issue: The firm was notified by a customer that the popcorn in the product contains...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2018· Signature Orthopedics Pty Limited

Recalled Item: Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature...

The Issue: This recall has been identified due to the batch being mislabeled, with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· 3M Company - Health Care Business

Recalled Item: 3M Surgical Clipper Professional 9681 Recalled by 3M Company - Health Care...

The Issue: Failure to follow proper charging practices can result in lithium-ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Merit Medical Systems, Inc.

Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...

The Issue: Supplier manufacturing defect with the syringe plunger tip.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 250 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope Power (Model 10967888) Recalled by Siemens Medical Solutions...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing