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. 2,465 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,465 in last 12 months

Showing 3262132640 of 49,976 recalls

Medical DeviceSeptember 2, 2016· Heritage Medical Products, Inc.

Recalled Item: 2000 Vascular with 30 Degree option Recalled by Heritage Medical Products,...

The Issue: Potential for bed to drop suddenly at the head while a patient is laying on it.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Arrow International Inc

Recalled Item: HANDS-OFF Infusion Port Thermodilution Catheter consists of the Arrow IPTD...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 1, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to RaySearch became...

The Issue: RaySearch became aware of the problem as it was discovered in cooperation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2016· Ormco/Sybronendo

Recalled Item: Sealapex Xpress Recalled by Ormco/Sybronendo Due to SybronEndo is recalling...

The Issue: SybronEndo is recalling the Sealapex Xpress because it was labeled with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Carry bar which is an accessory to a lift used Recalled by ErgoSafe...

The Issue: The black plastic puck on the carry bar is breaking resulting in potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
DrugAugust 30, 2016· Actavis Laboratories, FL, Inc.

Recalled Item: Ramipril Capsules Recalled by Actavis Laboratories, FL, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the...

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

Class III — Low RiskOngoing
Refund
FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Fudge Brownies - 20 muffins Recalled by BIMBO...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Variety - 20 pouches labeled for resale Recalled by...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· Snyder's-Lance Inc.

Recalled Item: Diamond of California¿ Macadamia Halves and Pieces 2.25oz packages Recalled...

The Issue: Product may be potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Chocolate Chip Muffins Recalled by BIMBO Bakeries...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· Snyder's-Lance Inc.

Recalled Item: Diamond of California¿ Chopped Macadamia Nuts 4oz Recalled by Snyder's-Lance...

The Issue: Product may be potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: ZENATANE (isotretinoin capsules USP) 20 mg Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew, Inc....

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Trimed Inc

Recalled Item: TriMed Semi-Tubular Plate Recalled by Trimed Inc Due to TriMed is recalling...

The Issue: TriMed is recalling the Semi-Tubular Plates with 10 holes (SMTP-10) because...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· ConMed Corporation

Recalled Item: CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter Recalled by ConMed...

The Issue: CONMED received complaints of damage to the CS-023 electrodes shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic V40 Femoral Head Recalled by Stryker Howmedica Osteonics Corp....

The Issue: Stryker received several complaints describing incidence of harm secondary...

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

Class II — Potential Health HazardOngoing