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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,642 in last 12 months

Showing 84618480 of 49,976 recalls

DrugJuly 5, 2023· B. Braun Medical Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc. Due to...

The Issue: Lack of assurance of sterility: bags have the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2023· Accord Healthcare, Inc.

Recalled Item: Bivalirudin for Injection 250 mg Recalled by Accord Healthcare, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter identified as fiber.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2023· Accord Healthcare, Inc.

Recalled Item: Atropine Sulfate Injection Recalled by Accord Healthcare, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter identified as fiber.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Total Hip Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The prep solution included in the Total Hip Kit expires prior to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2023· Philips Ultrasound, Inc.

Recalled Item: 3D9-3v Transducer Recalled by Philips Ultrasound, Inc. Due to Transducer, an...

The Issue: Transducer, an ultrasound system accessory, consists of two parts that are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2023· Cardiac Assist, Inc

Recalled Item: LifeSPARC Pump (part number 5800-0000) contained within TandemLife LifeSPARC...

The Issue: Epoxy used during manufacturing of the LifeSPARC Pump may have uncured...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Wireless Foot Switch distributed with Philips Allura Xper and Azurion...

The Issue: Loss of availability of the wireless foot switch during procedures.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2023· Abiomed, Inc.

Recalled Item: Impella RP Flex with SmartAssist intracardiac microaxial blood pump Recalled...

The Issue: A higher than expected rate of thrombus formation or deposition has been...

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

Class I — Serious Health HazardOngoing