Virginia Recalls

7,298 recalls on record affecting Virginia

Food Class II
2026-10-14

G L Mezzetta Inc recalls Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L.

Potential contamination with foreign objects: mice.

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drugs Class II
2026-10-07

Aurolab Trust recalls FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per via

Lack of Assurance of Sterility

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Food Class II
2026-10-07

LMSI, LLC recalls Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil,

Product contains garlic essential oil not approved for culinary use

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medical Class I
2026-09-23

Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150

this is a downstream recall of class I recall RES 98777

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medical Class I
2026-09-23

AVID Medical, Inc. recalls Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Ki

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

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medical Class I
2026-09-23

BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 508854

Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.

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medical Class I
2026-09-23

Bard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter, REF:

this is a downstream recall of class I recall RES 98777

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medical Class I
2026-09-23

AVID Medical, Inc. recalls Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

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medical Class I
2026-09-23

AVID Medical, Inc. recalls Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

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medical Class I
2026-09-23

AVID Medical, Inc. recalls Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit):

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

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Food Class II
2026-09-23

Best Friends Bakery, LLC recalls PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHO

Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.

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Food Class III
2026-09-23

Tiffany Food Corp recalls Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz cl

Unapproved dye Ponceau 4R

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medical Class I
2026-09-16

Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium C

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

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medical Class I
2026-09-16

Medical Action Industries, Inc. 306 recalls Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Sh

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

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Food Class I
2026-09-16

EURO FOODS GROUP USA NJ INC recalls Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 pack

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

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Food Class II
2026-09-09

Ukrop's Homestyle Foods LLC recalls Bread Pudding with Vanilla Sauce NET WT 13.8 OZ (39g) UPC 7

Foreign object: metal fragments

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Food Class II
2026-09-09

Ukrop's Homestyle Foods LLC recalls Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg)

Foreign object: metal fragments

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medical Class II
2026-08-26

SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068

Potential for electrical discharge from unit when unplugged.

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medical Class I
2026-08-26

Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK

After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy

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medical Class II
2026-08-26

Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGIC

Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing

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Showing 20 of 7,298 recalls. Use search to filter further.