Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,506 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,506 in last 12 months

Showing 3110131120 of 51,434 recalls

Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Remel Inc

Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...

The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: MP MUSCLEPHARM Recalled by Armada Nutrition Due to A raw material initially...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: Muscle Meds(TM) PERFORMANCE TECHNOLOGIES Recalled by Armada Nutrition Due to...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: MYPROTEIN Recalled by Armada Nutrition Due to A raw material initially...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: USN B4 -BOMB EXTREME PRE-WORKOUT Recalled by Armada Nutrition Due to A raw...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: BULK PRODUCT: MYPROTEIN Recalled by Armada Nutrition Due to A raw material...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: PERFORMIX(TM) CREA-BEAD Recalled by Armada Nutrition Due to A raw material...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2017· Armada Nutrition

Recalled Item: PERFORMIX(TM) CREA-BEAD Recalled by Armada Nutrition Due to A raw material...

The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 23, 2017· Toshiba American Medical Systems

Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...

The Issue: It was discovered during a procedure that when the operator made an exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Sysmex America Inc

Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...

The Issue: Reported customer complaints of automated hematology analyzers catching fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Merit Medical Systems, Inc.

Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...

The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund