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. 2,618 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,618 in last 12 months

Showing 94219440 of 28,127 recalls

Medical DeviceJune 14, 2021· Arthrex, Inc.

Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...

The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to The polyester-based...

The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 14, 2021· Philips Respironics, Inc.

Recalled Item: A-Series BiPAP A 40 Recalled by Philips Respironics, Inc. Due to The...

The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 14, 2021· Philips Respironics, Inc.

Recalled Item: A-Series BiPAP Hybrid A30 (not marketed in US) Recalled by Philips...

The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 10, 2021· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Arjo Citadel beds originally assembled with the IndiGo modules during...

The Issue: The IndiGo power cord might wear during use which could lead to its damage,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...

The Issue: There is a potential for >10% under-recovery on Activated Alanine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for 15%...

The Issue: There is a potential for 15% under-recovery on Activated Alanine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...

The Issue: There is a potential for >10% under-recovery on Activated Alanine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...

The Issue: There is a potential for >10% under-recovery on Activated Alanine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· GE OEC Medical Systems, Inc

Recalled Item: OEC 3D Imaging Recalled by GE OEC Medical Systems, Inc Due to There is a...

The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Merit Medical Systems, Inc.

Recalled Item: basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Recalled by...

The Issue: Due to a design issue, inflation syringe handle separating from the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· GE OEC Medical Systems, Inc

Recalled Item: OEC Elite mobile C-arm - Product Usage: intended to provide Recalled by GE...

The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Mercedes Medical, Inc.

Recalled Item: Lingen SAMPLE Disposable Virus Sampling Kit pack Recalled by Mercedes...

The Issue: No 510(k) clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2021· Mercedes Medical, Inc.

Recalled Item: Lingen Disposable Virus Sampling Kit Recalled by Mercedes Medical, Inc. Due...

The Issue: No 510(k) clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2021· Olympus Corporation of the Americas

Recalled Item: Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation...

The Issue: Expired adhesive used as an electrical insulation barrier and as a secondary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2021· Cardinal Health 200, LLC

Recalled Item: Infant Heel Warmer with Attachment Tab Recalled by Cardinal Health 200, LLC...

The Issue: A caution statement is being added to remind the user to activate away from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2021· Cardinal Health 200, LLC

Recalled Item: Infant Heel Warmer without Attachment Tab Recalled by Cardinal Health 200,...

The Issue: A caution statement is being added to remind the user to activate away from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2021· Cordis Corporation

Recalled Item: Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for...

The Issue: The product in the packaging is larger (both inner and outer diameter) than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728333 Spectral CT 7500 -Computed Tomography X-ray system Recalled by...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728332 IQon Spectral CT-Computed Tomography X-ray system Recalled by Philips...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing