The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

14951–14975 of 21645

  • ModerateFDA (Food)·F-0962-2016·2016-04-13

    Bj's Recalls Kunzler Sweet Bologna Due to Potential Cross-Contact

    Bj's Wholesale Club is recalling Kunzler Sweet Bologna deli items that may have been sliced on equipment used for pistachio mortadella.

    Product
    Kunzler Sweet Bologna, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-1014-2016·2016-04-13

    PerCoBa Colostrum Capsules Recalled for Incorrect Milk Allergen Labeling

    Immuno-Dynamics, Inc. is recalling PerCoBa Colostrum Capsules because the labels failed to state 'contains milk.' The product was distributed nationwide and internationally.

    Product
    PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) 1g. 120 capsules. UPC 90576-00011. Allergen statement: contains dairy. Distributed by: Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1042-2016·2016-04-13

    Novo Bnei Darom Green Olives Recalled for Unapproved Pesticide

    International Trading & Import Inc. is recalling Novo Bnei Darom Green Olives because they contain the unapproved pesticide Chlorpyrifos.

    Product
    Novo Bnei Darom Green Olives in Jar, 48 cases, 6 jars, 1.04kg, UPC Code 7290002016175
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0946-2016·2016-04-13

    Bj's Wholesale Club Recalls Peppered Ham Due to Cross-Contact Risk

    Bj's Wholesale Club is recalling D&W Peppered Ham sold in deli bags because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    D&W PEPPERED HAM, packaged in deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0952-2016·2016-04-13

    Bj's Wholesale Club Recalls Deli Ham Due to Cross-Contact Risk

    Bj's Wholesale Club is recalling DAK HAM sold in deli bags because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    DAK HAM, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0963-2016·2016-04-13

    Bj's Recalls Kunzler Lebanon Bologna Due to Cross-Contact Risk

    Bj's Wholesale Club is recalling Kunzler Lebanon Bologna because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    KUNZLER LEBANON BOLOGNA, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0981-2016·2016-04-13

    Bj's Wholesale Club Recalls Smoked Turkey Deli Slices

    Bj's Wholesale Club is recalling smoked turkey deli slices that may have been sliced on equipment used for pistachio-containing mortadella.

    Product
    WF SMOKED TURKEY, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-1021-2016·2016-04-13

    YumEarth Gummy Bears Recalled for Carbohydrate Labeling Error

    Yummy Earth Inc. is recalling YumEarth Organics Gummy Bears due to inconsistent carbohydrate labeling on the packaging.

    Product
    YumEarth Organics Gummy Bears 5 oz. Distributed by YummyEarth Inc., Ramsey, NJ 07446 UPC 810165018310
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0806-2016·2016-04-13

    Meditech Formula 3 Injection Recalled Due to Expired Active Ingredient

    Meditech Laboratories is recalling Formula 3 Injection vials because the active ingredient expired before the labeled Beyond Use Date.

    Product
    Formula 3 (Papaverine 20 mg, Phentolamine 3 mg, Atropine 0.2 mg, PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1041-2016·2016-04-13

    Abbott Nutrition Recalls PediaSure Grow & Gain Vanilla Due to Sensory Changes

    Abbott Nutrition is recalling PediaSure Grow & Gain Vanilla cans because the product may have an inconsistent color, smell, taste, or texture.

    Product
    The product is labeled as follows: PediaSure Grow & Gain Vanilla, Unit size : 8 oz. , Container description : Metal Can, Total package size : 24 cans per case .
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1015-2016·2016-04-13

    Immuno-Dynamics Recalls Colostrum Lozenges for Allergen Labeling Error

    Immuno-Dynamics, Inc. is recalling PerCoBa and Synertek colostrum lozenges because the labels state 'contains dairy' instead of 'contains milk.'

    Product
    Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the following sizes and Brand names: 1. PerCoBa, UPC 90576-00006. 100 Lozenges Distributed by: Immuno-Dynamics, Inc., Fennimore, WI 53809; 2.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0940-2016·2016-04-13

    Bj's Recalls D&W Gourmet Lite Ham for Cross-Contact Risk

    Bj's Wholesale Club is recalling D&W Gourmet Lite Ham sold in deli bags because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    D&W GOURMET LITE HAM, packaged in deli bag. This is a deli service item.
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0966-2016·2016-04-13

    Bj's Recalls Wellsley Farm Honey Turkey Deli Slices

    Bj's Wholesale Club is recalling Wellsley Farm Honey Turkey deli slices that may have been sliced on equipment used for mortadella with pistachios.

    Product
    WELLSLEY FARM HONEY TURKEY. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0958-2016·2016-04-13

    Bj's Wholesale Club Recalls Hormel Cooked Ham for Potential Cross-Contact

    Bj's Wholesale Club is recalling Hormel Cooked Ham sold in deli bags in eight states because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    HORMEL COOKED HAM, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1332-2016·2016-04-13

    Applied Medical Recalls Epix Universal Clip Appliers Due to Loading Defect

    Applied Medical Resources Corp is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.

    Product
    STD KIT GK260, Standard Set 360 Z Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1329-2016·2016-04-13

    Applied Medical Recalls Epix Universal Clip Appliers Due to Loading Mechanism Defect

    Applied Medical Resources Corp is recalling CA500 Epix Universal Clip Appliers due to a potential loading mechanism nonconformance. The recall affects 1,771 units distributed in the U.S. and internationally.

    Product
    CA500 Epix Universal Clip Applier Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1341-2016·2016-04-13

    Zimmer Persona Knee Implant Recalled for Box Labeling Discrepancy

    Zimmer Manufacturing B.V. is recalling specific Persona knee implants because the product box displayed conflicting part and lot numbers on different sides.

    Product
    Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in total knee arthroplasty. REF 42-5114-008-18
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Drugs)·D-0805-2016·2016-04-13

    Meditech Formula 1 Injection Recalled Due to Expired Active Ingredient

    Meditech Laboratories is recalling 1,320 vials of Formula 1 Injection because the active ingredient expired before the labeled Beyond Use Date.

    Product
    Formula 1 (Papaverine 1.8 mg, Phentolamine 0.2 mg, Atropine 0.02 mg, PGE 18 mcg/mL) Injection, 5 mL vial, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0948-2016·2016-04-13

    Bj's Recalls D&W Rotisserie Chicken Breast for Cross-Contact Risk

    Bj's Wholesale Club is recalling D&W Rotisserie Chicken Breast because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    D&W Rotissere Chicken Breast, packaged in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-0815-2016·2016-04-13

    Actavis Recalls Dextroamphetamine Tablets Due to Impurity Failures

    Actavis Elizabeth LLC is recalling 182,378 bottles of 30 mg Dextroamphetamine and Amphetamine tablets because they failed impurity specifications.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 30 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1022-2016·2016-04-13

    YumEarth Gummy Worms Recalled for Incorrect Carbohydrate Labeling

    Yummy Earth Inc. is recalling YumEarth Organics Gummy Worms because the outer and individual packages list different carbohydrate amounts.

    Product
    YumEarth Organics Gummy Worms Net Wt. 5 oz. Distributed by YummyEarth Inc., Ramsey, NJ 07446 UPC 810165018259
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0984-2016·2016-04-13

    BJ's Wholesale Club Recalls Deli Roast Beef for Cross-Contact Risk

    BJ's Wholesale Club is recalling deli roast beef sold in eight states because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    D&W Sandwich Ring substitute Roast Beef. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1330-2016·2016-04-13

    Applied Medical Resources Recalls Epix Universal Clip Applier Kits

    Applied Medical Resources Corp is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.

    Product
    STD GK258, AME Standard Kit 44 Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide