Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,428 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,428 in last 12 months

Showing 3414134160 of 49,990 recalls

Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Draeger Medical, Inc.

Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...

The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...

The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...

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

Class II — Potential Health HazardOngoing
FoodApril 21, 2016· Vitalicious Acquisition

Recalled Item: VitaTops Apple Crumb Recalled by Vitalicious Acquisition Due to Undeclared Milk

The Issue: The affected lots of VitaTops Apple Crumb contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 20, 2016· Liquid Assets Inc

Recalled Item: Life's Qik Fix 70 Plant Minerals Plus 80 Additional Nutrients Recalled by...

The Issue: Dietary Supplements contain undeclared milk and soy.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 20, 2016· Liquid Assets Inc

Recalled Item: Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging...

The Issue: Dietary Supplements contain undeclared milk and soy.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 20, 2016· Acorn Stairlifts, Inc

Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...

The Issue: The design of the seats did not consistently have the adequate strength...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Bupivacaine HCI 0.25% in 0.9% Sodium Chloride Recalled by Pharmakon...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Fentanyl Citrate 2 mcg/mL & Bupivacaine HCL 0.125 % in 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Potassium Chloride 40 mEq Added to 0.9% Sodium Chloride 250 mL bag Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Sufentanil Citrate 0.4mcg/mL & Bupivacaine 0.1% in 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Fentanyl Citrate 25 mcg/mL in 0.9% Sodium Chloride 25 mL in 30 mL syringe...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Oxytocin 20 Units added to 0.9% Sodium Chloride in a 1000mL lntravia bag...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Murray International Trading Co., Inc.

Recalled Item: PATCH-REMOUING PILL (For Facial Pigmentation) Recalled by Murray...

The Issue: Marketed Without An Approved NDA/ANDA: Products marked as dietary...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Hydromorphone HCI 0.4mg/mL in 0.9% Sodium Chloride 30 mL fill Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride 250 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Promethazine 12.5mg added to 0.9% Sodium Chloride 50 mL fill Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Hydromorphone HCI 0.2mg/mL in 0.9% Sodium Chloride 50 mL Cadd Cassette...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund