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. 2,420 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,420 in last 12 months

Showing 3810138120 of 50,914 recalls

Medical DeviceJune 30, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...

The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· BIOTRONIK, Inc.

Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...

The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2015· Qualitest Pharmaceuticals

Recalled Item: HydrOXYzine Hydrochloride Tablets Recalled by Qualitest Pharmaceuticals Due...

The Issue: Failed Tablet/Capsule Specifications; The identification codes on some...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Enterococcus Screen Agar QUAD Plate Recalled by Becton Dickinson & Co. Due...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to The...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter HomeChoice and HomeChoice Pro APD systems Recalled by Baxter...

The Issue: Loud operating sounds, which was unacceptable to the end users when the...

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2015· Merit Medical Systems, Inc.

Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or Recalled by...

The Issue: When using the CIVCO biopsy attachments in combination with the ACUSON S...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
FoodJune 27, 2015· Atkins Indiana Distribution Center

Recalled Item: Atkins Chocolate Candies  5 ct. cartons - code 637480075558 Recalled by...

The Issue: Atkins Nutritionals, Inc. is initiating a voluntary recall of a limited...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 27, 2015· Atkins Indiana Distribution Center

Recalled Item: Atkins Chocolate Peanut Candies 5 ct. Case - code 637480075770 Recalled by...

The Issue: Atkins Nutritionals, Inc. is initiating a voluntary recall of Cases of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2015· Ranbaxy Inc.

Recalled Item: Absorica (isotretinoin) Capsules Recalled by Ranbaxy Inc. Due to Undeclared...

The Issue: Incorrect/Undeclared Excipients: Product contains undeclared FD&C Yellow No....

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2015· American Health Packaging

Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...

The Issue: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted...

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

Class III — Low RiskOngoing
Refund