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 26461–26480 of 28,127 recalls
Recalled Item: Atricure Inc. Recalled by Atricure Inc Due to Products from lot no. 41865...
The Issue: Products from lot no. 41865 may have been sent out with Incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell...
The Issue: Out of an abundance of caution, Ansell is implementing a voluntary recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Sterile Polar Pads Recalled by Breg Inc Due to The recall was initiated...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and...
The Issue: VS2+ screen may lock up and stop monitoring during patient use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Cold Therapy Combination Units containing Sterile Polar Pads. 02356 Rev...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P10 Tobii battery box (product number 510410) Product Usage - Recalled by...
The Issue: Tobii ATI customers P10 external battery pack, which contains sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...
The Issue: The Dens Instrument Set has been designed to facilitate the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Combination Clamp/Large External Fixation System Recalled by Synthes...
The Issue: The L1 hex nuts, used to tighten the Large Combination Clamp, were oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left)...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Recalled by Synthes USA HQ, Inc. Due to It...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Grip which is part of the Synthes Universal Nail Recalled by...
The Issue: Synthes is initiating a voluntary recall of the Flexible Grip (Part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GHH51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MP Product Code:GMD51000000 Intended for use...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.