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 27081–27100 of 28,127 recalls
Recalled Item: Alloclassic¿ SL-Offset Stem sterile Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wagner SL Revision Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wagner cone Prosthesis Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30¿ Proximal positioner Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral Head Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul¿ LDH¿ Head Rx Sterile Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox¿ delta Ceramic Femoral Head Rx only Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Revision Humeral stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30 Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Inverse/Reverse Screw system Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Ball taper for humeral stem Recalled by Zimmer, Inc....
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...
The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 Recalled by Davol, Inc.,...
The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Ventralight ST Mesh. - Ellipse 7" x 9" (17.8 Recalled by Davol, Inc.,...
The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump Recalled...
The Issue: Accuro has received reports of some Apex Pumps either failing to operate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multipolar¿ Bipolar Cup Liner 22 mm LD. Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc. is initiating a removal of the Multipolar¿ Bipolar Cup Liner 22...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT Big Bore is a whole-body Computed Tomography Recalled by...
The Issue: Philips Healthcare received a complaint stating the system opens e-stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions, Inc., became aware of a potential problem involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System VARIABLE ANGLE SCREW MODULE...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.