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. 2,437 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,437 in last 12 months

Showing 3264132660 of 49,990 recalls

DrugSeptember 2, 2016· United Exchange Corporation

Recalled Item: EYE WASH Recalled by United Exchange Corporation Due to Lack of assurance of...

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
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
FoodSeptember 1, 2016· Interbake Foods

Recalled Item: Girl Scout Peanut Butter Sandwich Recalled by Interbake Foods Due to A...

The Issue: A single lot code of peanut butter used by the firm contained elevated...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 1, 2016· Interbake Foods

Recalled Item: Benton's Peanut Butter filled Cookies covered in Rich Fudge Recalled by...

The Issue: A single lot code of peanut butter used by the firm contained elevated...

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

Class II — Potential Health HazardOngoing
Refund
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
FoodAugust 31, 2016· Summit Import Corporation

Recalled Item: Yu Yee Brand Black Pepper Powder Recalled by Summit Import Corporation Due...

The Issue: Yu Yee Brand Black Pepper Powder may be 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· 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
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
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 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
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
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· 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· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
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· 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· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - Recalled by...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing