Hazard

Documentation recalls

38 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 38
Critical: 0
Severe: 1
Most recent: 2026-05-13

Of the 38 documentation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (3%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all documentation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

26–38 of 38

ModerateFDA (Devices)·Z-2808-2017·2017-08-16
FDA Recalls Hypodermic Needles Due to Insufficient Sterility Documentation
International Medsurg Connection, Inc. is recalling hypodermic needles because the company lacks sufficient documentation to support the product's sterility claims.
Product
Hypodermic Needle, 19 G X 1.0 in BD YALE DISP RG, 100 per box, 50 boxes/case, 5,000/case The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatme
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1236-2017·2017-03-01
Hidrex USA DP450 Medical Device Recalled for Documentation Requirements
Hidrex GmbH is recalling 64 units of the Hidrex USA DP450 device because it was reclassified from Class III to Class II, triggering new documentation requirements.
Product
Hidrex USA DP450
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1237-2017·2017-03-01
Hidrex USA DVP1000 Recalled Due to Documentation Requirements
Hidrex GmbH is recalling 180 units of the Hidrex USA DVP1000 device because it was reclassified from Class III to Class II, triggering new documentation requirements.
Product
Hidrex USA DVP1000
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0382-2016·2015-12-16
Skipanon Brand Canned Tuna Bellies Recalled for Documentation and Processing Concerns
Skipanon Brand Seafoods LLC is recalling approximately 57,000 cans of albacore tuna bellies due to lack of documentation and possible under-processing, which could lead to Clostridium botulinum contamination.
Product
Canned Albacore Tuna Bellies with paper label reading in part: ***SKIPANON BRAND SEAFOOD ALBACORE TUNA BELLIES or Ventresca***Ingredients: Albacore Tuna Bellies, Sea Salt, Spanish Olive Oil***NET WT. 66.5 OZ. (1885g)***" UPC: 58071 00145 Can code beginning with OCKB.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1306-2015·2015-08-12
Apothecary Shoppe Recalls SIU-Tri-Mix Due to Sterility Documentation Issues
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 20/1 mg/10 mcg/mL vials because proper environmental monitoring documentation was missing during production.
Product
SIU-Tri-Mix 20/1 mg/10 mcg/mL, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13452-2913-85
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-1302-2015·2015-08-12
Apothecary Shoppe Recalls SIU-Tri-Mix Injectable Due to Sterility Concerns
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 17/0.6/5.7 Injectable in Oklahoma due to lack of assurance of sterility from missing environmental monitoring documentation.
Product
SIU-Tri-Mix 17/0.6/5.7 Injectable, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-2348-22
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-1300-2015·2015-08-12
Apothecary Shoppe Recalls SIU-Phent Injection Due to Sterility Documentation Issues
The Apothecary Shoppe is recalling SIU-Phent .8/PGE1 20 mcg/mL Injection vials because proper environmental monitoring documentation was missing during production.
Product
SIU-Phent .8/PGE1 20 mcg/mL Inj., Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-2557-43
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-1316-2015·2015-08-12
Apothecary Shoppe Recalls S-Methylcobalamin Injection Due to Sterility Concerns
The Apothecary Shoppe LLC is recalling S-Methylcobalamin 5000 mcg/mL Injection in 750 mL containers due to a lack of assurance of sterility.
Product
S-Methylcobalamin 5000 mcg/mL Inj., Rx Only, 750 mL Container, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-1307-2015·2015-08-12
Apothecary Shoppe Recalls SIU-Tri-Mix Injection Due to Sterility Concerns
The Apothecary Shoppe is recalling SIU-Tri-Mix 24/1/20 Injection vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.
Product
SIU-Tri-Mix 24/1/20 Injection, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1747-39
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-1304-2015·2015-08-12
Apothecary Shoppe Recalls SIU-Tri-Mix Injection Due to Sterility Concerns
The Apothecary Shoppe is recalling SIU-Tri-Mix Injection Solution because proper environmental monitoring documentation was missing during production.
Product
SIU-Tri-Mix 6/0.33/3.33 Injection Solution, Rx Only, 3 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13429-2007-70
Category
Drug
Distribution
1 state
LowFDA (Devices)·Z-1597-2015·2015-05-20
Spinal Elements Mercury Lordosed Rods Recalled for Missing Traceability Markings
Spinal Elements, Inc. is recalling 588 Mercury lordosed rods because some lack required product identification markings, interrupting device traceability.
Product
Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprised of a variety of screws, hooks, rods, connectors, and staples that are used for attachment to the non-cervical spine. Rods span the distance between screws and hooks and achieve f
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0338-2014·2013-11-27
Synovis Recalls Vascu Guard and Dura-Guard Patches Due to Shipping Configuration Issues
Synovis is recalling Vascu Guard and Dura-Guard patches because specific fluid ounce units shipped in divided cell configurations with a specific revision of the Instructions for Use.
Product
Vascu Guard, Peripheral Vascular Patch with Apex Processing. For use in peripheral vascular reconstruction. Product Code: VG0106N VG0106N VG0106N VG0106N VG0106N VG0106N VG0106N VG0106N VG0106N VG0106N VG0106N VG010
Category
Medical Device
Distribution
Distributed nationwide
ModerateNHTSA·10T001000·2010-01-21
Yokohama Tires Recalled for Missing Identification Markings
Yokohama is recalling specific Avid H4S tires because they lack required identification markings on one sidewall, which could delay future safety repairs.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide