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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91387

7 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 17, 2022
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
MEDLINE INDUSTRIES, LP - Northfield

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

7 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 7

Non-sterile procedural trays labeled as CRANI, 2 per case

Z-1029-2023
Recall number
Z-1029-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
12 cases (24 units)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: DYNJ900413P, UDI/GTIN Case: 40195327031665, UDI/GTIN Each: 40195327031665, Lot Number: 22JDB689

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.

device · product 2 of 7

Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case

Z-1030-2023
Recall number
Z-1030-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
260 cases (520 units)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: DYNJ900415L, UDI/GTIN Case: 40195327029426, UDI/GTIN Each: 10195327029425, Lot Numbers: 22HBO658, 22JBV699

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.

device · product 3 of 7

Non-sterile procedural trays labeled as LAPAROTOMY CDS, 2 per case

Z-1031-2023
Recall number
Z-1031-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
57 cases (114 units)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: CDS980894A, UDI/GTIN Case: 40889942401292, UDI/GTIN Each: 10889942401291, Lot Numbers: 22HMD613, 22JMB665

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.

device · product 4 of 7

Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case

Z-1032-2023
Recall number
Z-1032-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
160 cases (480 units)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: DYNJ900416M, UDI/GTIN Case: 40195327031672, UDI/GTIN Each: 10195327031671, Lot Number: 22IBQ980

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.

device · product 5 of 7

Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case

Z-1033-2023
Recall number
Z-1033-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
216 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: DYNJ908295, UDI/GTIN Case: 40195327029570, UDI/GTIN Each: 10195327029579, Lot Numbers: 22IBN449, 22JBQ931

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.

device · product 6 of 7

Non-sterile procedural trays labeled as THEDA CLARK TOTAL KNEE CDS, 1 per case

Z-1034-2023
Recall number
Z-1034-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
45 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: CDSOPP508AG, UDI/GTIN Case: 40195327145140, UDI/GTIN Each: 10195327145149, Lot Number: 22HBO323

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.

device · product 7 of 7

Non-sterile procedural trays labeled as TOTAL KNEE KIT, 1 per case

Z-1035-2023
Recall number
Z-1035-2023
Initiated
November 17, 2022
Classification
Class II
Status
Ongoing
Quantity
16 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.

Code information

Item Number: DYNJ904310F, UDI/GTIN Case: 40195327116188, UDI/GTIN Each: 10195327116187, Lot Number: 22IBD724;

Distribution pattern

US Nationwide distribution in the states of AR, MD, WA, WI.