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. 1,740 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,740 in last 12 months

Showing 4244142460 of 50,914 recalls

DrugJune 27, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: LORTUSS EX Recalled by Poly Pharmaceuticals, Inc Due to Does Not Meet...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: POLY-TUSSIN AC LIQUID Recalled by Poly Pharmaceuticals, Inc Due to Does Not...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 26, 2014· Biosound Esaote, Inc.

Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...

The Issue: Using the PA230E transducer with a user-defined setting with the output...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Alphatec Spine, Inc.

Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Hill-Rom, Inc.

Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...

The Issue: The attachment latch mechanism can become bent depending on user handling....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Salter Labs

Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...

The Issue: The case label correctly states partial rebreather but the insert label...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Karl Storz Endoscopy

Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...

The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2014· Zimmer, Inc.

Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...

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

Class II — Potential Health HazardOngoing
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Lipo 8 Injection USP 200 mg/ml Recalled by Medical Supply Liquidators Llc...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Glutathione Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: G.A.C. 375 Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B6 Pyridoxine HCL for Injection USP Recalled by Medical Supply...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Cyanocobalamin with MIC Injection USP 1000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Hydroxocobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin with MIC Injection USP 1000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Cyanocobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: MIC Injection USP Recalled by Medical Supply Liquidators Llc Due to Marketed...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund