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 2196121980 of 49,976 recalls

Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: Battery short-run times and unanticipated stoppage may be due to user not...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Mizkan America, Inc. - Corporate

Recalled Item: Ragu Old World Style Sauce Flavored with Meat 66oz retail Recalled by Mizkan...

The Issue: foreign material

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Mizkan America, Inc. - Corporate

Recalled Item: Ragu Chunky Sauce Tomato Recalled by Mizkan America, Inc. - Corporate Due to...

The Issue: foreign material

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Mizkan America, Inc. - Corporate

Recalled Item: Ragu Old World Style Sauce Traditional 66oz retail size sold in plastic jar...

The Issue: foreign material

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Sprout's Farmers Market

Recalled Item: Sprouts Farmers Market Cut Leaf Spinach Recalled by Sprout's Farmers Market...

The Issue: Testing revealed the presence of Listeria monocytogenes in the frozen spinach

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Sprout's Farmers Market

Recalled Item: Sprouts Farmers Market Organic Cut Leaf Spinach Recalled by Sprout's Farmers...

The Issue: Testing revealed the presence of Listeria monocytogenes in the frozen spinach

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 14, 2019· TELEFLEX-MORRISVILLE

Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...

The Issue: Device vented gas below the stated pressure.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 14, 2019· Stanley Security Solutions Inc

Recalled Item: STANLEY Healthcare Arial 54315 Network Manager Recalled by Stanley Security...

The Issue: STANLEY Healthcare has received reports of outages on the Arial nurse call...

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

Class II — Potential Health HazardOngoing
DrugJune 13, 2019· B. Braun Medical Inc

Recalled Item: Heparin Sodium 25 Recalled by B. Braun Medical Inc Due to Subpotent Drug:...

The Issue: Subpotent Drug: low out-of-specification results were identified for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 13, 2019· Baxter Healthcare Corporation

Recalled Item: Sevoflurane Recalled by Baxter Healthcare Corporation Due to Failed...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Topical Solution 30mg of testosterone per pump actuation *...

The Issue: Defective Container; actuator may improperly function and affect dose delivery.

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

Class III — Low RiskOngoing
Refund