Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93395

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

Open FDA event record

Event summary

Timeline bucket
November 03, 2023
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

STERILE PVP SOLUTION, REF DYNDA1907

Z-0525-2024
Recall number
Z-0525-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
8250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40889942574491 (case), 10889942574490 (each), Lot numbers: 22LBL675, 22JBR599, 22IBS045, 22GBT655, 22DBN398, 22DBD250, 22DBA001, 21LBN032, 21JBA478, 21EBE405

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

device · product 2 of 7

STERILE PVP SLN KIT, REF DYNDM1097

Z-0526-2024
Recall number
Z-0526-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
100 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40884389601892 (case), 10884389601891 (each), Lot numbers: 21GBJ087

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

device · product 3 of 7

STERILE STERILE PREP STICK, REF DYNDA1134

Z-0527-2024
Recall number
Z-0527-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
240 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40888277098023 (case), 10888277098022 (each), Lot numbers: 2023082190

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

device · product 4 of 7

STERILE PVP, REF DYNDA1649

Z-0528-2024
Recall number
Z-0528-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
700 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40889942326519 (case), 10889942326518 (each), Lot numbers: 2022060190, 2022021590

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

device · product 5 of 7

PVP SOLUTION SING STRL, REF DYNDA1858

Z-0529-2024
Recall number
Z-0529-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
1950 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40889942539858 (case), 10889942539857 (each), Lot numbers: 2023032090, 2023020990, 2022103190, 2022091690, 2022070190, 2022052090, 2022042290, 2022033190, 2021102290, 2021092190

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

device · product 6 of 7

STERILE BETADINE, REF DYNDA1998

Z-0530-2024
Recall number
Z-0530-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
1800 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40889942651062 (case), 10889942651061 (each), Lot numbers: 2023042190, 2022101090, 2022081590, 2022041390, 2022031090, 2022011290, 2021100490

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

device · product 7 of 7

STERILE POVIDONE, REF DYNDA2061

Z-0531-2024
Recall number
Z-0531-2024
Initiated
November 03, 2023
Classification
Class II
Status
Ongoing
Quantity
300 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

Code information

UDI/DI 40889942697633 (case), 10889942697632 (each), Lot numbers: 2022040790, 2022062190

Distribution pattern

US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.

Field note

Send feedback

We'll only use this to respond to your feedback.