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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 88046

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

Open FDA event record

Event summary

Timeline bucket
May 21, 2021
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Cardinal Health 200, LLC

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

8 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 8

Sterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2031-2021
Recall number
Z-2031-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
574 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

Lot Numbers: 20LJS033, 20MJS072

Distribution pattern

US Nationwide distribution.

device · product 2 of 8

Nonsterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2032-2021
Recall number
Z-2032-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
26250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

Lot Numbers: 0141ER1, 0141ER2, 2400ER2, 2410ER1, 2410ER2, 2540ER2, 2550ER1, 2550ER2, 2580ER1, 2580ER2, 2590ER1, 2590ER2, 2600ER1, 2760ER2, 2880ER1, 2940ER1, 2940ER2, 3070ER1, 3080ER1, 3530ER1, 3530ER2

Distribution pattern

US Nationwide distribution.

device · product 3 of 8

Sterile Radial/Femoral Angiography Drape, Catalog Number 29529 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2033-2021
Recall number
Z-2033-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
3192 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

Lot Numbers: 20HGR063, 20JGR059, 20JGR068, 20JGR094, 20KGR048, 20LGR074

Distribution pattern

US Nationwide distribution.

device · product 4 of 8

Nonsterile Radial/Femoral Angiography Drape, Catalog Number 29529N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2034-2021
Recall number
Z-2034-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
13426 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

Lot Numbers: 2320DR1, 2330DR1, 2410DR1, 2440DR1, 2450DR1, 2580DR1, 2670DR1, 2730DR1, 2740DR1, 2790DR1, 2830DR1, 2860DR1, 2870DR1, 2890DR1, 2900DR1, 2930DR1, 2940DR1, 2950DR1, 3080DR1, 3310DR1, 3320DR1, 3330DR1, 3350DR1

Distribution pattern

US Nationwide distribution.

device · product 5 of 8

Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2035-2021
Recall number
Z-2035-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
1638 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

Lot Numbers: 20LRR092, 20MRR079

Distribution pattern

US Nationwide distribution.

device · product 6 of 8

Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2036-2021
Recall number
Z-2036-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
6461 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

Lot Numbers: 0121QR2, 0391RR1, 3070QR1, 3280QR1, 3280QR2, 3290QR1, 3290QR2, 3300QR1, 3300QR2, 3310QR1, 3310QR2, 3320QR1, 3570QR1, 3570QR2

Distribution pattern

US Nationwide distribution.

device · product 7 of 8

Sterile Femoral Angiography Drape, Catalog Numbers: a) 29460, b) 29456 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2037-2021
Recall number
Z-2037-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
5342 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

a) 29460: Lot Numbers: 20LRS055, 20MRS073, 21ARS042 b) 29456: Lot Numbers: 20MMR062

Distribution pattern

US Nationwide distribution.

device · product 8 of 8

Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Z-2038-2021
Recall number
Z-2038-2021
Initiated
May 21, 2021
Classification
Class II
Status
Terminated
Recalling firm
Cardinal Health 200, LLC
Quantity
15360 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Code information

a) 29460NB: Lot Numbers: 0071PR1, 0121PR1, 0131PR1, 0141PR1, 0271PR1, 0281PR1, 0291PR1, 0351PR1, 0361PR1, 0391PR1, 0401PR1, 3040PR1, 3110PR1, 3250PR1, 3380PR1, 3510PR1, 3520PR1, 3530PR1 b) 29456NB: Lot Numbers: 3290LR1, 3300LR1, 3310LR1, 3320LR1, 3350LR1, 3390LR1, 3420LR1

Distribution pattern

US Nationwide distribution.