Recall events
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Event 87954
Event summary
Timeline bucket May 11, 2021
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Medical Action Industries, Inc. 306
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
5 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 5
Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
Z-1945-2021
Recall number Z-1945-2021
Initiated May 11, 2021
Classification Class II
Status Terminated
Quantity 23 boxes of 20 devices
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1945-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4883]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Code information Batch Number 0000274502, Expiration Date 07/24/2025
Distribution pattern US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34137]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 5
Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224
Z-1946-2021
Recall number Z-1946-2021
Initiated May 11, 2021
Classification Class II
Status Terminated
Quantity 97 boxes of 20 devices
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1946-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[21748]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Code information Batch Numbers: 0000277592, Exp. 10/12/2025; 0000274266, Exp. 07/21/2025; 0000275098, Exp. 08/21/2025; 0000276380, Exp. 09/24/2025
Distribution pattern US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[32628]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 5
novaplus, General Purpose Kit, Cat. No. 56603
Z-1947-2021
Recall number Z-1947-2021
Initiated May 11, 2021
Classification Class II
Status Terminated
Quantity 21 cases of 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1947-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33477]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Code information Batch Numbers: 0000275724, Exp. 02/15/2022; 0000277619, Exp. 04/15/2022
Distribution pattern US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[35130]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 5
Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209
Z-1948-2021
Recall number Z-1948-2021
Initiated May 11, 2021
Classification Class II
Status Terminated
Quantity 102 cases of 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1948-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15565]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Code information Batch Numbers: 0000277610, Exp. 04/15/2022; 0000276879, Exp. 04/15/2022
Distribution pattern US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34102]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 5
Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214
Z-1949-2021
Recall number Z-1949-2021
Initiated May 11, 2021
Classification Class II
Status Terminated
Quantity 31 cases of 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1949-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[58301]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Code information Batch Numbers: 0000275137, Exp. 05/29/2022; 0000276914, Exp. 02/01/2023
Distribution pattern US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[35137]
FDA event record
· Exact recall-number query on openFDA
