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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,509 in last 12 months

Showing 1996119980 of 28,654 recalls

Medical DeviceJuly 8, 2016· Nakanishi Inc.

Recalled Item: Diamond Coated Tips and Burs are accessories to the air Recalled by...

The Issue: Through an error, the labeling failed to include the symbol or other text...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 45CM Item Code: E277345 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire L-Hook Electrode 28CM Item Code: E278328 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Blade Electrodes 28CM...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 28CM Item Code: E278228 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277236 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Cylindrical Tip Electrode 28CM Item Code: E278628 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode 36CM Item Code: E277436 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Nakanishi Inc.

Recalled Item: Diamond Coated Tips and Burs are accessories to the Ultrasonic Recalled by...

The Issue: Through an error, the labeling failed to include the symbol or other text...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· BioMerieux SA

Recalled Item: NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products...

The Issue: Several customer complaints about amplification performance issues when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2016· Elekta, Inc.

Recalled Item: Medical Linear Accelerator Recalled by Elekta, Inc. Due to There have been...

The Issue: There have been instances in hospitals where the joint between the drive...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Arrow International Inc

Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...

The Issue: Arrow is recalling due to incorrect labeling of products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· TZ Medical, Inc.

Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...

The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Siemens Medical Solutions USA, Inc

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

The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...

The Issue: This field action is being initiated following the firm's discovery of a...

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

Class III — Low RiskOngoing