Device recall: BD MaxGuard Extension Set with 4-way stopcock, REF: M4058
Class II FDA enforcement event 90707. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.
Class II, in the words of FDA
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
CAREFUSION started this device recall on 1 Aug 2022. The firm address in the FDA record is in San Diego, CA. FDA put the recall in Class II. FDA event 90707 has 9 product records. The first FDA enforcement report date is 28 Sep 2022. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN
Recalling firm
CAREFUSION, San Diego, CA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
9 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1752-2022 | BD MaxGuard Extension Set with 4-way stopcock, REF: M4058 | 46,900 | Class II | Ongoing | 28 Sep 2022 |
| Z-1753-2022 | BD MaxGuard Extension Set, REF: ME1069 | 3,500 | Class II | Ongoing | 28 Sep 2022 |
| Z-1754-2022 | BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106 | 54,050 | Class II | Ongoing | 28 Sep 2022 |
| Z-1755-2022 | BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141 | 37,550 | Class II | Ongoing | 28 Sep 2022 |
| Z-1756-2022 | BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436 | 19,925 | Class II | Ongoing | 28 Sep 2022 |
| Z-1757-2022 | BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059 | 17,250 | Class II | Ongoing | 28 Sep 2022 |
| Z-1758-2022 | BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166 | 600 | Class II | Ongoing | 28 Sep 2022 |
| Z-1759-2022 | BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171 | 100 | Class II | Ongoing | 28 Sep 2022 |
| Z-1760-2022 | BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433 | 9,900 | Class II | Ongoing | 28 Sep 2022 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2022
- 839
- Share of these events in Class II
- 88%
- Product records in this event
- 9Median of the firm: 9
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 2 Aug 2021 | BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E | Device | Class II | 15 |
| 9 Jun 2021 | MaxPlusTM bi fuse extension set with 2 clear needleless connectors - Product Usage: The needleless connector can be used | Device | Class II | 1 |
Official channels
- FDA enforcement report Z-1752-2022The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Cite this page
Recall Register. FDA enforcement event 90707. https://recallregister.com/fda/ii/90707/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN
- What quantity of product is in FDA event 90707?
- The event has 9 product records. The first record gives this quantity:
46,900
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2022 have the same class?
- 88% of the 839 device events that started in 2022 are in Class II.