Exact FDA event identifier

Event 82212

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

Event summary

Timeline bucket: February 08, 2019
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Terumo Medical Corporation

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

9 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 9

Terumo Sur-vet Needle, 20G x 1", Product Code 100204

Z-1998-2019

Recall number: Z-1998-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 729,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180709C, 180915C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 2 of 9

Terumo Sur-vet Needle, 22G x 1", Product Code 100211

Z-1999-2019

Recall number: Z-1999-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 444,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180710C, 180717C, 181015C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 3 of 9

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215

Z-2000-2019

Recall number: Z-2000-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 638,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180720C 180810C 180830C 181006C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 4 of 9

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220

Z-2001-2019

Recall number: Z-2001-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 440,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180706C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 5 of 9

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279

Z-2002-2019

Recall number: Z-2002-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 844,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180705C 180814C 180829C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 6 of 9

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280

Z-2003-2019

Recall number: Z-2003-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 563,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180814C 181002C 181009C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 7 of 9

Terumo Needle, 18G x 1", Product Code NN1825R

Z-2004-2019

Recall number: Z-2004-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 810,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180714C, 180723C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 8 of 9

Terumo Needle, 23G x 1", Product Code NN2325R

Z-2005-2019

Recall number: Z-2005-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 30,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 180811C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

device · product 9 of 9

Terumo Needle, 30G x 1/2", Product Code NN3013R

Z-2006-2019

Recall number: Z-2006-2019
Initiated: February 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: Terumo Medical Corporation
Quantity: 81,000

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

package integrity that may compromise

Sterility assurance reason.sterility_assurance · v1.0.0

package integrity that may compromise the sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Code information

Lot Numbers 181005C

Distribution pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.