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 27321–27340 of 28,127 recalls
Recalled Item: ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroCool Breathable Gown with Towels Recalled by Kimberly-Clark Corporation...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aviator Drill Bit (10 mm Recalled by Stryker Spine Due to Aviator drill bits...
The Issue: Aviator drill bits are 10 mm longer than the Hybrid drill bits and are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL software version 6.12 for the ABL800 analyzer. The Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL software version 6.12 for the ABL800 and ABL700 Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith &...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BP7561 OPTI CCA-TS B-Lac Cassette (25 per box) Cassettes are Recalled by...
The Issue: The values reported for PCO2 by BP7561 B-Lac cassettes are biased at high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545...
The Issue: Three complaints have been filed where the Hoffman LRF Telescopic Struts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verify¿ Bowie-Dick Test Card Recalled by Steris Corporation Due to STERIS...
The Issue: STERIS has learned that the Verify Bowie Dick Test Cards are not performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is Recalled by...
The Issue: The IntraOs 70 system was found to have missing or incomplete system labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian ARIA Oncology Information System Recalled by Varian...
The Issue: A software anomaly has been identified with the Import Export Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Blanket Protective Coverlet Recalled by Beekley Corporation Due to...
The Issue: Imaging artifact can occur on mammogram result
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY LIQUIBEADS Vaginal Moisturizer Recalled by Mc-NEIL-PPC, Inc. Due to...
The Issue: Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Philips Healthcare was notified that several of the sixteen bolts securing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix...
The Issue: Ethicon and Omrix Biopharmaceuticals have received reports of air or gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc....
The Issue: A routine internal quality check found that the Drager PT 4000 Phototherapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.