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. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 26281–26300 of 28,127 recalls
Recalled Item: Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge Recalled by...
The Issue: Straight needle labeled as a curved needle
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160....
The Issue: Labeling Revision: Additional instructions for the use of peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Extra Short (4") with Recalled by...
The Issue: Labeling Revision: Additional instructions for the use of peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Recalled by...
The Issue: Labeling Revision: Additional instructions for the use of peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended...
The Issue: Labeling Revision: Additional instructions for the use of peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214...
The Issue: Glucose test strips reports no result message when tested
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeScan brand OneTouch¿ Ultra Control Solution Recalled by Lifescan Inc Due...
The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to...
The Issue: Meter kit outer boxes containing 10 ct. test strips state incorrect storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeScan brand OneTouch¿ Select Control Solution Recalled by Lifescan Inc...
The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReClaim Reamer Extension Recalled by DePuy Orthopaedics, Inc. Due to The...
The Issue: The tabs on the reamer extension device have broken. DePuy is notifying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOPump Elastometric infusion PumpKit with/ and without accesssories all...
The Issue: Received 2 complaints out of 458 distributed pumps in this lot, where flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog #...
The Issue: Glucose test strips reports no result message when tested
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Tri-Level Multi-Parameter Assayed Hematology Control Recalled...
The Issue: Elevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments....
The Issue: Stryker received reports from the field indicating that the handle detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 11-Hole Recalled by Synthes USA HQ, Inc. Due to The Synthes...
The Issue: The Synthes One-Third Tubular DCL Plate (11-Hole, 1/3 Tubular Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerr Maxcem Elite Recalled by Kerr/Pentron, DBA Kerr Corporation and Pentron...
The Issue: Kerr Corporation is initiating this recall because raw material used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Radial Head Prosthesis: Trial Radial Head Elbow joint prosthesis:...
The Issue: The Trial Head may come loose from the implant stem during manipulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aperio ScanScope System. Aperio ScanScope Models Recalled by Aperio...
The Issue: Aperio initiated this recall because the User Guides incorrectly state the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension(R) Phosphorus (PHOS) Flex(R) reagent cartridge (DF61) The...
The Issue: Siemens Healthcare Diagnostics has initiated a voluntary field action for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoSelect DBM Putty Product Usage: Orthopedic bone filler Recalled by...
The Issue: The firm's retesting procedure was not validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.