Allergen Hub

Fish Recalls in the United States

9578 food recalls involving fish tracked from FDA open data. Updated daily.

9578 Fish Recalls

All food recalls →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441,

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP, Pump Set C

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 100

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Set, Pump Set Code 0048-0044; containing

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella RP Flex with SmartAssist Set, Pump Set Code

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Introducer Kit 14 Fr, 25 cm, Pump Set Cod

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Set, Pump Set Code 0048-0014; containing

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP;

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Introducer Kit 14 Fr, 13 and 25 cm, Pump

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Introducer Kit 14 Fr, 13 cm, Pump Set Cod

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class I
2026-07-22

Abiomed, Inc. recalls ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

View recall details →
medical Class II
2026-07-15

Integra LifeSciences Corp. (NeuroSciences) recalls OmniTract Surgical Retractor System, which includes 633 of t

The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.

View recall details →
medical Class II
2026-07-15

Think Surgical, Inc. recalls TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090

Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.

View recall details →
medical Class II
2026-07-15

WALLAC OY recalls GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010.

Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.

View recall details →
drugs Class II
2026-07-15

QuVa Pharma, Inc. recalls Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume:

Failed Impurities/Degradation Specifications

View recall details →
Food Class I
2026-07-15

Fresh & Ready Foods LLC recalls Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10

Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

View recall details →
Food Class I
2026-07-15

Fresh & Ready Foods LLC recalls Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz.

Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

View recall details →
Food Class I
2026-07-15

Trafa Pharmaceutical Inc. recalls Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER

Potential contamination with Salmonella

View recall details →