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. 936 recalls have been distributed to Iowa in the last 12 months.
Showing 44721–44740 of 49,990 recalls
Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...
The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Vision Mounting Arm Recalled by Stryker Endoscopy Due to When...
The Issue: When positioning the display located on top of the video cart, it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus" Head (Not distributed in the United States) Recalled by Zimmer, Inc....
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys¿ Beaded Fullcoat Femoral Stem (POR FULL-CT FEM ST 11X160MM Recalled...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: There are artifacts appearing on the Tracker images during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul¿ Head. Intended for use either with or without bone Recalled by...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender Solutions" Patello-Femoral Component Recalled by Zimmer, Inc. Due to...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...
The Issue: Imprecision with certain lots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF POR FEM Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vented Spike Adapter Product Code 2C0471 Recalled by Baxter Healthcare Corp....
The Issue: Potential tears in the pouch of six lots of Vented Spike Adapter Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...
The Issue: Defective Container: Defective bottles may not have tamper evident seals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...
The Issue: Presence of Foreign Substance: This recall is being conducted due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter; Glass particulates observed in vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter; report of visible particulates in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...
The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.