Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,458 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,458 in last 12 months

Showing 3472134740 of 49,976 recalls

Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P3 Kodel. Pediatric sized vest is Recalled by Ossur H /...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is Recalled by Ossur H /...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV MST-30 Kit under the following labels: 1) 4F Recalled...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Sorbatex. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV IR-145 Kit under the following labels: 1) 4F Recalled...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 9 (Papaverine 0.9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 0 (PGE 20 mcg/mL) Injection Recalled by Meditech Laboratories, Inc...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Superpotent Drug: one ingredient was found to be above assay specification.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 4 (Papaverine 18 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 3 (Papaverine 20 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...

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

Class II — Potential Health HazardOngoing
Refund