Recall Register

Food, drugs, devices › Covidien LLC

Device recall: Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill Product ID: 8881570121 Product Usage: Both 0.

FDA enforcement event 65978 · Class II · initiated 16 Aug 2013 · status Terminated · terminated 21 Oct 2015

DeviceVoluntary: Firm initiated9 product recordsMansfield, MA

Covidien LLC (Mansfield, MA) initiated this device recall on 16 Aug 2013; FDA lists 9 product records under event 65978, classified Class II.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 90% of the 1,236 device enforcement events initiated in 2013 carry the same class.

Status: Terminated, terminated 21 Oct 2015. Initiation: voluntary: firm initiated. Covidien LLC has 77 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Covidien LLC, Mansfield, MA.

Reason for recall

"Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin"

Distribution

"Worldwide Distribution - USA Nationwide and the country of Bermuda"

Product records

Recall numberProductQuantityClassStatusReport date
Z-2178-2013Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 10 mL Fill Product ID: 8881570121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…3,235,860 unitsClass IITerminated18 Sep 2013
Z-2179-2013Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 3 mL Fill Product ID: 8881570123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2180-2013Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 5 mL Fill Product ID: 8881570125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2181-2013Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID:8881580121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2182-2013Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881580123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2183-2013Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881580125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2184-2013Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID: 8881590121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2185-2013Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881590123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…UnknownClass IITerminated18 Sep 2013
Z-2186-2013Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881590125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous…330,120 unitsClass IITerminated18 Sep 2013

Context

90%of 2013 device events are Class II1,236 events that year
9product records in this eventfirm median: 1
77events on this register for the firm

Other enforcement events for Covidien LLC

InitiatedProduct (first record)TypeClassRecords
13 May 2026EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFDeviceClass II1
23 Apr 2026Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042DeviceClass II3
23 Apr 2026Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the CovidiDeviceClass II1
15 Apr 2026COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028 The devices are intendeDeviceClass II1
30 Jan 2026HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 MDeviceClass II1
25 Apr 2024EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx OnlyDeviceClass II1
2 Jun 2023Covidien Cytosponge Cell Collection Device, REF: CYTO-201; and Covidien Cytosponge Cell Collection Kit, REF: CYTO-KIT-USDeviceClass II1
22 May 2023Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CSDeviceClass II1
23 Nov 2022COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1DeviceClass II1
19 Aug 2022Puritan Bennett 560 Ventilator, PB560, CFN 4096600DeviceClass II1

All 77 events for Covidien LLC

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin"

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "Worldwide Distribution - USA Nationwide and the country of Bermuda"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 21 Oct 2015. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.