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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85502

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

Open FDA event record

Event summary

Timeline bucket
April 13, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
American Contract Systems

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

14 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 14

Sterile Custom Packs to be used in surgical procedures.

Z-2166-2020
Recall number
Z-2166-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2,868 surgical kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: SVOH98F; Lot # 676191, Exp. date 11/20/20 (3 kits) AHMV261; Lot # 676191, Exp. date 11/20/20 (10 kits) AGMV26L: Lot # 688191, Exp. date 11/08/2020 (36 kits) FBTO60G: Lot # 635191, Exp. date 12/31/2020 (25 kits) FBTO60G: Lot # 711191, Exp. date 10/16/2020 (3 kits) AGEP48G: Lot # 991201, Exp. date 01/09/2021 (72 kits) AGBR90D: Lot # 843191, Exp. date 06/06/2020 (48 kits) AGTP52J: Lot # 643191, Exp. date 12/23/2020 (42 kits) AGTP52J: Lot # 716191, Exp. date 10/11/2020 (8 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 2 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2167-2020
Recall number
Z-2167-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2,868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGCY21I; Lot # 664191, Exp. date 12/02/20 (72 kits) WXCY21F; Lot # 661191, Exp. date 12/05/20 (32 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 3 of 14

Custom Packs to be used in surgical procedures.

Z-2168-2020
Recall number
Z-2168-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2, 868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

WPGA21L; Lot # 998201, Exp. Date 01/02/2021 (24 kits) and Lot # 6781914, Exp date 11/18/2020 (4 kits) AGGL48H; Lot# 643191, Exp. Date 12/23/2020 (80 kits) AGGM59N: Lot # 761191, Exp. Date 08/27/2020 (5 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 4 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2169-2020
Recall number
Z-2169-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2, 868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: FBPL271; Lot # 656191, Exp. Date 12/10/2020 (32 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 5 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2170-2020
Recall number
Z-2170-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2,868 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: WPPP52E; Lot # 723191, Exp. Date 10/04/2020 (24 kits) AGMM60M; Lot # 656191, Exp. Date 12/10/2020 (20 kits) VSMI14G; Lot # 643191, Exp. Date 12/23/2020 (60) and Lot #71891, Exp. Date 10/09/2020 (6 kits) WXOLO48H; Lot # 654191, Exp. Date 12/12/2020 (6 kits) AGKD5OJ; Lot # 997201, Exp. Date 01/03/2021 (26 kits) AGME44J; Lot # 997201, Exp. Date 01/03/2021 (24 kits) AGMA31K; Lot # 642191, Exp. Date 12/24/2020 (96 kits) AGMI141; Lot # 671191, Exp. Date 11/25/2020 (36 kits) and Lot # 789191, Exp. Date 07/30/2020 (14 kits) AVMA31I; Lot # 675191, Exp. Date 11/21/2020 (2 kits) AVMI14H; Lot # 639191, Exp. Date 12/27/2020 (70 kits) WXMI14H; Lot # 650191, Exp. Date 12/16/2020 (160 kits) AGLO48H; Lot # 670191, Exp. Date 11/26/2020 (30 kits) SVMA21I; Lot # 654191, Exp. Date 12/12/2020 (30 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 6 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2171-2020
Recall number
Z-2171-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGLH66F; Lot # 674191, Exp. Date [date] (244 kits) AGAD45I; Lot# 681191, Exp. Date 11/15/2020 (35 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 7 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2172-2020
Recall number
Z-2172-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2868 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGD1401; Lot # 647191, Exp. Date 06/31/2020 (72 kits) and Lot # 685191 Exp. Date 03/31/2020 (6 kits) WPP147H; Lot # 684191, Exp. Date 11/12/2020 (20 kits) and Lot # 723191 Exp. Date 10/04/2020 (4 kits) SVOH38N; Lot # 654191, Exp. Date 12/12/2020 (32 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 8 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2173-2020
Recall number
Z-2173-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGTA481; Lot # 998201, Exp. Date 01/02/2021 (60 kits) WXEN11G; Lot # 994201, Exp. Date 01/06/2021 (32 kits) VSMT20G; Lot # 677191, Exp. Date 11/19/2020 (12 kits) AGHN20J; Lot # 636191, Exp. Date 12/30/2020 (4 kits); Lot # 675191, Exp. Date 11/21/2020 (12 kits) and Lot # 741191, Exp. Date 09/16/2020 (36 kits) AGEN11H; Lot # 657191, Exp. Date 12/09/2020 (66 kits) VSEN11F; Lot # 664191, Exp. Date 12/02/2020 (8 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 9 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2174-2020
Recall number
Z-2174-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: FBCS38I; Lot # 692191, Exp. Date 11/04/2020 (4 kits) and Lot # 648191,Exp. Date 12/18/2020 (40 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 10 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2175-2020
Recall number
Z-2175-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2,868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGMV151; Lot # 993201, Exp. Date 01/07/2021 (12 kits) and Lot # 676191,Exp. Date 11/20/2020 (18 kits) WXMV15H; Lot # 663191, Exp. Date 12/03/2020 (32 kits) AGLA66H; Lot # 675191, Exp. Date 11/21/2020 (4 kits) AGLP521; Lot # 648191, Exp. Date 12/18/2020 (6 kits) AGVA31H; Lot # 675191, Exp. Date 11/21/2020 (6 kits) AGIF04F; Lot # 683191, Exp. Date 11/13/2020 (50 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 11 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2176-2020
Recall number
Z-2176-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGSBOO6K; Lot # 660191, Exp. Date 12/06/2020 (19 kits) AGDB14J; Lot # 737191, Exp. Date 09/20/2020 (2 kits) AHLA17J; Lot # 653191, Exp. Date 12/13/2020 (12 kits) SVNE16K; Lot # 691191, Exp. Date 11/05/2020 (20 kits) WPLA17I; Lot # 685191, Exp. Date 11/11/2020 (2 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 12 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2177-2020
Recall number
Z-2177-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2,8,68 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: WXCT12E; Lot # 998201, Exp. Date 001/02/2021 (70 kits) PTHS10C; Lot # 664191, Exp. Date 12/02/2020 (2 kits) AVHA64H; Lot # 663191, Exp. Date 12/06/2020 (30 kits) WXPO16G; Lot # 639191, Exp. Date 12/27/2020 (26 kits) and Lot # 689191, Exp. Date 11/07/2020 (6 kits) VSSA12G; Lot # 646191, Exp. Date 12/20/2020 (12 kits) AGBA20H: Lot 3 970191, Exp. Date 01/30/20 (2 kits) WXSA12H; Lot # 653191, Exp. Date 12/13/2020 (40 kits) WXKA26H; Lot # 981201, Exp. Date 01/19/2021 (18 kits) and Lot # 639191, Exp. Date 12/27/2020 (32 kits) WXHA64H; Lot # 682191, Exp. Date 11/14/2020 (18 kits); Lot # 636191, Exp. Date 12/30/2020 (121 kits) and Lot # 684191, Exp. Date 11/12/2020 (6 kits) AGKA26H; Lot # 992201, Exp. Date 01/08/2021 (64 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 13 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2178-2020
Recall number
Z-2178-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2, 868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AGPP38I; Lot # 644191, Exp. Date 12/22/2020 (2 kits) and Lot # 713191, Exp. Date 10/14/2020 (12 kits) AGHA64J; Lot # 663191, Exp. Date 12/03/2020 (72 kits) and Lot # 716191, Exp. Date 10/11/2020 (10 kits) WPBU64H; Lot # 670191, Exp. Date 11/26/2020 (16 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

device · product 14 of 14

Sterile Custom Packs to be used in surgical procedures.

Z-2179-2020
Recall number
Z-2179-2020
Initiated
April 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
American Contract Systems
Quantity
2,868 total kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The surgical gowns were manufactured in a facility that is not registered by the FDA.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Code information

ACS Tray Numbers: AVLC19G; Lot # 642191, Exp. Date 12/24/2020 (64 kits)

Distribution pattern

US Nationwide distribution including in the state of Pennsylvania.

Field note

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